Skip to main content
SpringerLink
Log in

Families of Dothideomycetes

In loving memory of Majorie Phyllis Hyde (affectionately known as Mum or Marj), 29 August 1921–18 January 2013—without mum’s determination, a character passed on to children, this treatise would never have been completed—K.D. Hyde

  • Published:
Fungal Diversity Aims and scope Submit manuscript

Abstract

Dothideomycetes comprise a highly diverse range of fungi characterized mainly by asci with two wall layers (bitunicate asci) and often with fissitunicate dehiscence. Many species are saprobes, with many asexual states comprising important plant pathogens. They are also endophytes, epiphytes, fungicolous, lichenized, or lichenicolous fungi. They occur in terrestrial, freshwater and marine habitats in almost every part of the world. We accept 105 families in Dothideomycetes with the new families Anteagloniaceae, Bambusicolaceae, Biatriosporaceae, Lichenoconiaceae, Muyocopronaceae, Paranectriellaceae, Roussoellaceae, Salsugineaceae, Seynesiopeltidaceae and Thyridariaceae introduced in this paper. Each family is provided with a description and notes, including asexual and asexual states, and if more than one genus is included, the type genus is also characterized. Each family is provided with at least one figure-plate, usually illustrating the type genus, a list of accepted genera, including asexual genera, and a key to these genera. A phylogenetic tree based on four gene combined analysis add support for 64 of the families and 22 orders, including the novel orders, Dyfrolomycetales, Lichenoconiales, Lichenotheliales, Monoblastiales, Natipusillales, Phaeotrichales and Strigulales. The paper is expected to provide a working document on Dothideomycetes which can be modified as new data comes to light. It is hoped that by illustrating types we provide stimulation and interest so that more work is carried out in this remarkable group of fungi.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10
Fig. 11
Fig. 12
Fig. 13
Fig. 14
Fig. 15
Fig. 16
Fig. 17
Fig. 18
Fig. 19
Fig. 20
Fig. 21
Fig. 22
Fig. 23
Fig. 24
Fig. 25
Fig. 26
Fig. 27
Fig. 28
Fig. 29
Fig. 30
Fig. 31
Fig. 32
Fig. 33
Fig. 34
Fig. 35
Fig. 36
Fig. 37
Fig. 38
Fig. 39
Fig. 40
Fig. 41
Fig. 42
Fig. 43
Fig. 44
Fig. 45
Fig. 46
Fig. 47
Fig. 48
Fig 49
Fig. 50
Fig. 51
Fig. 52
Fig. 53
Fig. 54
Fig. 55
Fig. 56
Fig. 57
Fig. 58
Fig. 59
Fig. 60
Fig. 61
Fig. 62
Fig. 63
Fig. 64
Fig. 65
Fig. 66
Fig. 67
Fig. 68
Fig. 69
Fig. 70
Fig. 71
Fig. 72
Fig. 73
Fig. 74
Fig. 75
Fig. 76
Fig. 77
Fig. 78
Fig. 79
Fig. 80
Fig. 81
Fig. 82
Fig. 83
Fig. 84
Fig. 85
Fig. 86
Fig. 87
Fig. 88
Fig. 89
Fig. 90
Fig. 91
Fig. 92
Fig. 93
Fig. 94
Fig. 95
Fig. 96
Fig. 97
Fig. 98
Fig. 99
Fig. 100
Fig. 101
Fig. 102
Fig. 103
Fig. 104
Fig. 105
Fig. 106
Fig. 107
Fig. 108
Fig. 109
Fig. 110
Fig. 111
Fig. 112
Fig. 113
Fig. 114
Fig. 115
Fig. 116
Fig. 117
Fig. 118
Fig. 119
Fig. 120
Fig. 121
Fig. 122
Fig. 123
Fig. 124
Fig. 125
Fig. 126
Fig. 127
Fig. 128
Fig. 129
Fig. 130
Fig. 131
Fig. 132
Fig. 133
Fig. 134
Fig. 135
Fig. 136
Fig. 137
Fig. 138
Fig. 139
Fig. 140
Fig. 141
Fig. 142

Similar content being viewed by others

References

  • Abarca GH, Ruiz RFC, Mota RMA, Hernandez CIB, Gomez S, Bogale M, Untereiner WA (2011) A new species of Heliocephala from Mexico with an assessment of the systematic position of the anamorph genera Heliocephala and Holubovaniella. Mycologia 103:631–640

    PubMed  Google Scholar 

  • Abdel-Aziz FA, Abdel-Wahab MA (2010) Lolia aquatica gen. et sp. nov. (Lindgomycetaceae, Pleosporales), a new coelomycete from freshwater habitats in Egypt. Mycotaxon 114:33–42

    Google Scholar 

  • Abdel-Wahab A, Jones EGB (2000) Three new marine ascomycetes from driftwood in Australia sand dunes. Mycoscience 41:379–388

    Google Scholar 

  • Abdollahzadeh J, Goltapeh EM, Javadi A, Shams-Bakhsh M, Zare R, Phillips AJL (2009) Barriopsis iraniana and Phaeobotryon cupressi: two new species of the Botryosphaeriaceae from trees in Iran. Persoonia 23:1–8

    CAS  PubMed Central  PubMed  Google Scholar 

  • Abler SW (2003) Ecology and Taxonomy of Leptosphaerulina spp. associated with Turfgrasses in the United States. Masters Thesis. Blacksburg, Virginia

  • Acharius E (1798) Lichenographiae. Suecicae Prodromus, Linköping

    Google Scholar 

  • Aguirre-Hudson B (1991) A taxonomic study of the species referred to the ascomycete genus Leptorhaphis. Bulletin of the British Museum (Natural History). Botany 21:85–192

    Google Scholar 

  • Aguirre-Hudson B (2009) Celothelium, Cresporhaphis, Leptorhaphis, Rhaphidicyrtis. In: Smith CW et al (eds) The lichens of Great Britain and Ireland. The British Lichen Society, MPG Books Group, Bodmin

    Google Scholar 

  • Aguirre-Hudson B, Fiol L (1993) A new species of Leptorhaphis (Arthopyreniaceae) on Opuntia from the Balearic Islands. Lichenologist 25:207–210

    Google Scholar 

  • Aguirre-Hudson B, Hawksworth DL (1987) The circumscription, biology and relationships of the genus Leptorhaphis Körber. In: Peveling E (ed) Progress and problems in Lichenology in the eighties. Bibliotheca Lichenologica 25:249–255

  • Aguirre-Hudson B, Farkas E, Lokös L (2002) Pyrenolichens of the Hungarian lichen flora I: The genus Leptrorhaphis Körber. Bibl Lichenologica 82:3–18

    Google Scholar 

  • Ahmed SI, Asad F (1968) Sporormia fimicola sp. nov. and Sporormiella inaequalis sp. nov. from West Pakistan. Sydowia 21:290–294

    Google Scholar 

  • Ahmed SI, Cain RF (1972) Revision of the genera Sporormia and Sporormiella. Can J Bot 50:419–477

    Google Scholar 

  • Ainsworth GC, James PW, Hawksworth DL (1971) Ainsworth & Bisby’s dictionary of the fungi, 6th edn. CAB, Kew

    Google Scholar 

  • Alexopoulos CJ, Mims CW, Blackwell M (1996) Introductory mycology. Wiley, New York

    Google Scholar 

  • Alias SA, Jones EBG (2009) Marine fungi from mangroves of Malaysia. Institute of Ocean and Earth Sciences, University Malaya, p 108

  • Alstrup V, Kocourkova J, Kukwa M, Motiejunaite J, von Brackel W, Suija A (2009) The lichens and lichenicolous fungi of South Greenland. Folia Cryptog Estonica 46:1–24

    Google Scholar 

  • Andjic V, Barber PA, Carnegie AJ, Hardy GSJ, Wingfield MJ, Burgessa TI (2007) Phylogenetic reassessment supports accommodation of phaeophleospora and Colletogloeopsis from eucalypts in kirramyces. Mycol Res 111:1184–1198

    Google Scholar 

  • Aptroot A (1991a) A monograph of the Pyrenulaceae (excluding Anthracothecium and Pyrenula) and the Requienellaceae, with notes on the Pleomassariaceae, the Trypetheliaceae and Mycomicrothelia (lichenized and non–lichenized Ascomycetes). Bibl Lichenologica 44:1–178

    Google Scholar 

  • Aptroot A (1991b) Monoblastia pellucida: a remarkable new lichen species from tropical coastal areas, with comments on the Monoblastiaceae. Bryologist 94:404–406

    Google Scholar 

  • Aptroot A (1995a) A monograph of Didymosphaeria. Stud Mycol 37:1–160

    Google Scholar 

  • Aptroot A (1995b) Redisposition of some species excluded from Didymosphaeria (Ascomycetes). Nova Hedwigia 60:325–379

    Google Scholar 

  • Aptroot A (1998) A world revision of Massarina (Ascomycota). Nova Hedwigia 66:89–162

    Google Scholar 

  • Aptroot A (1999) Notes on the taxonomy, distribution and ecology of Anisomeridium polypori. Lichenologist 31:641–642

    Google Scholar 

  • Aptroot A (2002a) Acrocordia. In: Nash TH III, Ryan BD, Gries C, Bungartz F (eds) Lichen flora of the Greater Sonoran Desert Region. I. Lichens unlimited. Arizona State University, Tempe, p 89

    Google Scholar 

  • Aptroot A (2002b) Mycoporum. In: Nash TH III, Ryan BD, Gries C, Bungartz F (eds) Lichen Flora of the Greater Sonoran Desert Region, vol I. Lichens unlimited. Arizona State University, Tempe, pp 287–288

    Google Scholar 

  • Aptroot A (2002c) Tomasellia. In: Nash TH III, Ryan BD, Gries C, Bungartz F (eds) Lichen flora of the Greater Sonoran Desert Region, vol I. Lichens unlimited. Arizona State University, Tempe, pp 487–488

    Google Scholar 

  • Aptroot A (2003) Pyrenocarpous lichens and related non–lichenized ascomycetes from Taiwan. J Hattori Bot Lab 93:155–173

    Google Scholar 

  • Aptroot A (2006) Mycosphaerella and its anamorphs 2. Conspectus of Mycosphaerella. CBS Biodiversity Series 5:1–231

  • Aptroot A (2012) A world key to the species of Anthracothecium and Pyrenula. Lichenologist 44:5–53

    Google Scholar 

  • Aptroot A, Sipman HJM (1993) Musaespora, a genus of pyrenocarpous lichens with campylidia, and other additions to the foliicolous lichen flora of New Guinea. Lichenologist 25:121–135

    Google Scholar 

  • Aptroot A, Sipman HJM (2001) New Hong Kong lichens, ascomycetes and lichenicolous fungi. J Hattori Bot Lab 91:317–343

    Google Scholar 

  • Aptroot A, van Iperen AL (1998) New ascomycetes and ascomycete records from Papua New Guinea. Nova Hedwigia 67:481–497

    Google Scholar 

  • Aptroot A, Diederich P, Sérusiaux E, Sipman HJM (1995) Lichens and lichenicolous fungi of Laing Island (Papua New Guinea). Bibl Lichenologica 57:19–48

    Google Scholar 

  • Aptroot A, Diederich P, Sérusiaux E, Sipman HJM (1997) Lichens and lichenicolous fungi from New Guinea. Bibl Lichenologica 64:1–220

    Google Scholar 

  • Aptroot A, Lücking R, Sipman HJM, Umaña L, Chaves JL (2008) Pyrenocarpous lichens with bitunicate asci: a first assessment of the lichen biodiversity inventory in Costa Rica. Bibl Lichenologica 97:1–162

    Google Scholar 

  • Ariyawansa HA, Jones EBG, Suetrong S, Alias SA, Kang JC, Hyde KD (2013a) Halojulellaceae a new family of the order Pleosporales. Phytotaxa 130:14–24

    Google Scholar 

  • Ariyawansa HA, Maharachchikumbura SSN, Karunarathne SC, Chukeatirote E, Bahkali AH, Kang JC, Bhat JD, Hyde KD (2013b) Deniquelata barringtoniae from Barringtoniaasiatica, associated with leaf spots of Barringtonia asiatica. Phytotaxa 105:11–20

    Google Scholar 

  • Arnaud G (1913) Sur les genres Zopfia, Richonia et Caryospora. Bull Trimest Soc Mycol Fr 29:253–260

    Google Scholar 

  • Arnaud G (1915) Notes mycologiques (G. Isaria et Parodiopsis). Bull Soc Mycol Fr 31(1):20–23

    Google Scholar 

  • Arnaud G (1918) Les Astérinées. Ann Ecole Nat Agric Montpellier nouv Série 16:1–288

    Google Scholar 

  • Arnaud G (1920) La famille des Parodiellinacées (Pyrénomycètes). C R Acad Sci 170:202–204

    Google Scholar 

  • Arnaud G (1921) Les Astérinées: II. Études sur les champignons (Parodiellinacées, inclus Erysiphées). Ann Epiphyties 7:1–115

    Google Scholar 

  • Arnaud G (1925) Les Asterinees. IVe Partie. (Études sur la Systématique des champignons Pyrénomycetes). Annales Des Sciences Naturelles. Botanique 7:643–723

    Google Scholar 

  • Arnaud G (1930) Les Astérinées. V. Études sur les champignons parasites: Caliciacées, Hémisphériacées, etc. Ann Épiphyties 16:235–302

    Google Scholar 

  • Arnaud G (1931) Traité de PathologieVégétal, Paris, vol. 1, 2

  • Arnold F (1858) Die Lichenen des fränkischen Jura. Flora 41:81–95

    Google Scholar 

  • Arzanlou M, Groenewald JZ, Gams W, Braun U, Shin H-D, Crous PW (2007) Phylogenetic and morphotaxonomic revision of Ramichloridium and allied genera. Stud Mycol 58:57–93

    CAS  PubMed Central  PubMed  Google Scholar 

  • Atkinson GF (1902) New genera of the higher fungi. Bot Gaz 34(1):36–43

    Google Scholar 

  • Auerswald B (1866) Delitschia nov. gen. e grege Sphaeriacearum simplicium. Hedwigia 5:49–64

    Google Scholar 

  • Aveskamp MM, de Gruyter J, Crous PW (2008) Biology and recent developments in the systematic of Phoma, a complex genus of major quarantine significance. Fungal Divers 31:363–382

    Google Scholar 

  • Aveskamp MM, de Gruyter H, Woudenberg J, Verkley G, Crous PW (2010) Highlights of the Didymellaceae: a polyphasic approach to characterise Phoma and related pleosporalean genera. Stud Mycol 65:1–60

    CAS  PubMed Central  PubMed  Google Scholar 

  • Barnes I, Crous PW, Wingfield BD, Wingfield MJ (2004) Multigene phylogenies reveal that red band needle blight of Pinus is caused by two distinct species of Dothistroma, D. septosporum and D. pini. Stud Mycol 50:551–565

    Google Scholar 

  • Barr ME (1961) Northern pyrenomycetes. II. Gaspesian Park. Can J Bot 39:307–325

    Google Scholar 

  • Barr ME (1968) The Venturiaceae in North America. Can J Bot 46(6):799–864

    Google Scholar 

  • Barr ME (1975) The genus Ostreichnion. Mycotaxon 3:81–88

    Google Scholar 

  • Barr ME (1976) Perspectives in the Ascomycotina. Mem N Y Bot Gard 28:1–8

    Google Scholar 

  • Barr ME (1979a) A classification of Loculoascomycetes. Mycologia 71:935–957

    Google Scholar 

  • Barr ME (1979b) On the Massariaceae in North America. Mycotaxon 9:17–37

    Google Scholar 

  • Barr ME (1980) On the family Tubeufiaceae (Pleosporales). Mycotaxon 12:137–167

    Google Scholar 

  • Barr ME (1981) The genus Curreya: an example of taxonomic confusion in the Ascomycetes. Mycologia 73:599–609

    Google Scholar 

  • Barr ME (1982) On the Pleomassariaceae (Pleosporales) in North America. Mycotaxon 15:349–383

    Google Scholar 

  • Barr ME (1983a) Muriform ascospores in class Ascomycetes. Mycotaxon 18:149–157

    Google Scholar 

  • Barr ME (1983b) The ascomycete connection. Mycologia 75:1–13

    Google Scholar 

  • Barr ME (1987a) Prodomus to class Loculoascomycetes. Publ. by theauthor, Amherst

    Google Scholar 

  • Barr ME (1987b) New taxa and combinations in the Loculoascomycetes. Mycotaxon 29:501–505

    Google Scholar 

  • Barr ME (1987c) Prodromus to class Loculoascomycetes. University of Massachusetts, Amherst

    Google Scholar 

  • Barr ME (1989a) Some unitunicate taxa excluded from Didymosphaeria. Stud Mycol 31:23–27

    Google Scholar 

  • Barr ME (1989b) The genus Dothidotthia (Botryosphaeriaceae) in North America. Mycotaxon 34:517–526

    Google Scholar 

  • Barr ME (1990a) Melanommatales (Loculoascomycetes). N Am Flora Ser II 13:1–129

    Google Scholar 

  • Barr ME (1990b) Prodromus to nonlichenized, pyrenomycetous members of class Hymenoascomycetes. Mycotaxon 39:43–184

    Google Scholar 

  • Barr ME (1990c) Some dictyosporous genera and species of Pleosporales in North America. Mem N Y Bot Gard 62:1–92

    Google Scholar 

  • Barr ME (1990d) Melanommatales (Loculoascomycetes). N Am Flora 2:1–129

    Google Scholar 

  • Barr ME (1992a) Additions to and notes on the Phaeosphaeriaceae (Pleosporales, Loculoascomycetes). Mycotaxon 43:371–400

    Google Scholar 

  • Barr ME (1992b) Notes on the Lophiostomataceae (Pleosporales). Mycotaxon 45:191–221

    Google Scholar 

  • Barr ME (1993a) Notes on the Pleomassariaceae. Mycotaxon 49:129–142

    Google Scholar 

  • Barr ME (1993b) Redisposition of some taxa described by J. B. Ellis. Mycotaxon 46:4576

    Google Scholar 

  • Barr ME (1996) Planistromellaceae, a new family in the Dothideales. Mycotaxon 60:433–442

    Google Scholar 

  • Barr ME (1997) Notes on some ‘dimeriaceous’ fungi. Mycotaxon 64:149–171

    Google Scholar 

  • Barr ME (2000a) Notes on coprophilous bitunicate ascomycetes. Mycotaxon 76:105–112

    Google Scholar 

  • Barr ME (2000b) Teichosporaceae, another family in the Pleosporales. Mycotaxon 82:373–389

    Google Scholar 

  • Barr ME (2001) Montagnulaceae, a new family in Pleosporales, and lectotypification of Didymosphaeriella. Mycotaxon 77:193–200

    Google Scholar 

  • Barr ME (2002) Teichosporaceae, another family in the Pleosporales. Mycologia 82:373–389

    Google Scholar 

  • Barr ME (2003) The affinities of Thyridaria. Mycotaxon 88:271–278

    Google Scholar 

  • Barr ME, Blackwell M (1980) A new genus in the Lophiaceae. Mycologia 72:1224–1227

    Google Scholar 

  • Barr ME, Huhndorf SM (2001) Loculoascomycetes. In: McLaughlin DJ, McLaughlin EG, Lemke PA (eds) The mycota VII, part A. Systematics and evolution. Springer Verlag, Berlin, pp 283–305

    Google Scholar 

  • Batista AC (1957) The Atichiales in Pernambuco. Anais Soc Biol Pernamb 15:311–332

    Google Scholar 

  • Batista AC (1959) Monografia dos fungos Micropeltaceae. Publicações Inst Micol Univ Recife 56:1–519

    Google Scholar 

  • Batista AC (1960) Lembopodia, Yamamotoa e Peresiopsis, novos gêneros de Asterinaceae. Publ IMUR, Recife 291:1–35

    Google Scholar 

  • Batista AC, Cavalcante W d A (1967) Acanthorus n.gen. e outros Coelomycetes de fumagina. Atas do Instituto de Micologia. Univ Pernambuco, Recife 4:245–254

    Google Scholar 

  • Batista AC, Ciferri R (1957) Two previously undescribed cucurbitariaceous fungi. Atti dell’Istituto. Botanico dell’Universita di Pavia 5(15):63–66

    Google Scholar 

  • Batista AC, Ciferri R (1963) The sooty-molds of the family Asbolisiaceae. Quaderni. Laboratorio Crittogamico, Istituto Botanico della Università di Pavia 31:7, p 229

    Google Scholar 

  • Batista AC, Maia HDS (1965) Caprettia, novo genero de ascoliquen, em homenagem ao micologo venezuelano, Corrado Capretti. Univ Fed Pernambuco Inst Micol Atas 2:375–382

    Google Scholar 

  • Batista AC, Nascimento ML (1957) Alguns novos fungos imperfeitos do complex de fumagina. An Soc Biol Pernambuco 15(2):345–353

    Google Scholar 

  • Batista AC, Maia HS, Farr ML (1958) Novos generos e novasespecies de fungos Asterinaceae. Rev Biol Lisbõa 1(3–4):287–298

    Google Scholar 

  • Batista AC, Bezerra JL, de Cavalcante W d A, da Silva MH (1963) Mycerema e outros novos gêneros de Stomiopeltoideae, da familia Micropeltaceae. Publicações Inst Micol Univ Recife 392:1–40

    Google Scholar 

  • Batzer JC, Mercedes Diaz Arias M, Harrington TC, Gleason ML, Groenewald JZ, Crous PW (2008) Four species of Zygophiala (Schizothyriaceae, Capnodiales) are associated with the sooty blotch and flyspeck complex on apple. Mycologia 100:246–258

    CAS  PubMed  Google Scholar 

  • Behrend G (1890) Ueber Trichomycosis nodosa (Juhel-Renoy); Piedra (Osorio). 27:464–467

  • Bensch K, Braun U, Groenewald JZ, Crous PW (2012) The genus Cladosporium. Stud Mycol 72:1–401

    CAS  PubMed Central  PubMed  Google Scholar 

  • Berkeley MJ (1845) Decades of fungi. Decades III-VII. Australian fungi. London J Bot 4:42–73

    Google Scholar 

  • Berkeley MJ (1876) Notices of North American fungi. Grevillea 4(31):105–106

    Google Scholar 

  • Berkeley MJ, Broome CE (1850) Notices of British fungi (438–501). Ann Mag Nat Hist 5:455–466

    Google Scholar 

  • Berlese AN (1896) Icones fungorum. II. fasc: 29–68

  • Berlese A (1900) Icones Fungorum. Padova 2:216

    Google Scholar 

  • Bin S (2003) Goosia, a new genus of Englerulaceae. Mycotaxon 87:413–415

    Google Scholar 

  • Bisby GR (1923) The literature on the classification of the Hysteriales. Trans Br Mycol Soc 8:176–189

    Google Scholar 

  • Bizzozero G (1885) Funghi Veneti novi vel critici. Atti dell’Istituto Veneto Scienze 3:303

    Google Scholar 

  • Blackwell M, Gilbertson RL (1985) Quasiconcha reticulata and its anamorph from conifer roots. Mycologia 77:50–54

    Google Scholar 

  • Blain WL (1927) Comparative morphology of dothideaceous and kindred stromata. Mycologia 19(1):13

    Google Scholar 

  • Boedijn KB (1961) Myriangiales from Indonesia. Persoonia 2:63–75

    Google Scholar 

  • Boehm E, Mugambi G, Miller A, Huhndorf S, Marincowitz S, Spatafora J (2009a) A class–wide phylogenetic assessment of Dothideomycetes. Stud Mycol 64:1–15S10

    PubMed Central  PubMed  Google Scholar 

  • Boehm EWA, Mugambi G, Miller AN, Huhndorf S, Marincowitz S, Schoch CL, Spatafora JW (2009b) A phylogenetic reappraisal of the Hysteriaceae, Mytilinidiaceae & Gloniaceae with keys to world species. Stud Mycol 64:49–83

    CAS  PubMed Central  PubMed  Google Scholar 

  • Boehm EWA, Schoch CL, Spatafora JW (2009c) On the evolution of the Hysteriaceae and Mytilinidiaceae (Pleosporomycetidae, Dothideomycetes, Ascomycota) using four nuclear genes. Mycol Res 113:461–479

    CAS  PubMed  Google Scholar 

  • Boerema GH (1997) Contributions towards a monograph of Phoma(Coelomycetes) - V. Subdivision of the genus in sections. Mycotaxon 64:321–333

    Google Scholar 

  • Boerema GH, De Gruyter J, Noordeloos ME, Hamers MEC (2004) Phomaidentification manual. Differentiation of specific and infraspecific taxa in culture. CABI Publishing, United Kingdom

    Google Scholar 

  • Boise JR (1985a) An amended description of Trematosphaeria. Mycologia 77:230–237

    Google Scholar 

  • Boise JR (1985b) New combinations in the Pleomassariaceae and the Massarinaceae. Mycotaxon 22:477–482

    Google Scholar 

  • Boissière JC, Montavont JP (1998) Lichens de France (XI): Epigloea filifera Döbb. et Lobaria amplissima (Scop.) Forss. dans sa forme avec céphalodies. Bull d’Informations l’Assoc Française Lichénologie 23(1):1–6

    Google Scholar 

  • Bonifaz A, Badali H, de Hoog GS, Cruz M, Araiza J (2008) Tinea nigra by Hortaea werneckii, a report of 22 cases from Mexico. Stud Mycol 61:77–82

    CAS  PubMed Central  PubMed  Google Scholar 

  • Boonmee S, Zhang Y, Chomnunti P, Chukeatirote E, Tsui CKM, Bahkali AH, Hyde KD (2011) Revision of lignicolous Tubeufiaceae based on morphological reexamination and phylogenetic analysis. Fungal Divers 51:63–102

    Google Scholar 

  • Boonmee S, KoKo TW, Chukeatirote E, Hyde KD, Chen H, Cai L, McKenzie EHC, Jones EBG, Kodsueb R, Hassan BA (2012) Two new Kirschsteiniothelia species with Dendryphiopsis anamorphs cluster in Kirschsteiniotheliaceae fam. nov. Mycologia 104:698–714

    PubMed  Google Scholar 

  • Boonmee et al. (2013) Tubeufiales, ord. nov., integrating sexual and asexual generic names (in prep)

  • Borse BD (1987) Marine fungi from India, V. Curr Sci 56:1109–1111

    Google Scholar 

  • Bose SK (1961) Studies on Massarina Sacc. and related genera. Phytopathol Z 41:151–213

    Google Scholar 

  • Brandriff H (1936) The development of the ascocarp of Acrospermum compressum. Mycologia 28:228–235

    Google Scholar 

  • Braun U (1995) A monograph of Cercosporella, Ramularia and allied genera (Phytopathogenic Hyphomycetes). Vol. 1. IHW–Verlag, Eching

    Google Scholar 

  • Braun U (1998) A monograph of Cercosporella, Ramularia and allied genera (Phytopathogenic Hyphomycetes). Vol. 2. IHW–Verlag, Eching

    Google Scholar 

  • Braun U, Crous PW, Dugan F, Groenewald JZ, de Hoog GS (2003) Mycol Prog 2:3–18

    Google Scholar 

  • Braun U, Crous PW, Schubert K, Shin HD (2010) Some reallocations of Stenella species in Zasmidium. Schlechtendalia 20:99–104

    Google Scholar 

  • Braun-Falco O, Plewig G, Wolff HH, Burgdorf WHC (2000) Dermatology, 2nd edn. Springer Verlag, Berlin

    Google Scholar 

  • Brefeld O (1891) Unter suchungen aus dem gesammtge biete der Mycologie. 10. Ascomyceten. II. Münster. p 378

  • Breuss O (2001) Flechten aus Costa Rica II. Linzer Biologische Beitraege 33:1025–1034

    Google Scholar 

  • Bricaud O, Roux C, Ménard T, Coste C (1993) Champignons lichénisés et lichénicoles de la France méridionale: espèces nouvelles et intéressantes (8). Bull Société Linnéenne de Provence 44:99–109

    Google Scholar 

  • Burney DA, Robinson GS, Burney LP (2003) Sporormiella and the late Holocene extinctions in Madagascar. Proc Natl Acad Sci U S A 100:10800–10805

    CAS  PubMed Central  PubMed  Google Scholar 

  • Bussaban B, Lumyong S, Lumyong P, Seelanan T, Park D, McKenzie E, Hyde K (2005) Molecular and morphological characterization of Pyricularia and allied genera. Mycologia 97(5):1002–1011

    CAS  PubMed  Google Scholar 

  • Cai L, Guo XY, Hyde KD (2008) Morphological and molecular characterisation of a new anamorphic genus Cheirosporium, from freshwater in China. Persoonia 20:53–58

    CAS  PubMed Central  PubMed  Google Scholar 

  • Cain RF (1934) Studies of coprophilous Sphaeriales in Ontario. Univ Toronto Stud: Biol Ser 38:1–126

    Google Scholar 

  • Cain RF (1956) Studies on coprophilous ascomycetes. II. Phaeotrichum, a new cleistocarpous genus in a new family, and its relationships. Can J Bot 34:675–684

    Google Scholar 

  • Calatayud V, Navarro-Rosinés P (1998) Weddellomyces xanthoparmeliae sp. nov. and additions to the chorology of other species of the genus. Mycotaxon 69:503–514

    Google Scholar 

  • Calatayud V, Triebel D (2003) Three new species of Stigmidiums. l. (lichenicolous ascomycetes) on Acarospora and Squamarina. Lichenologist 35(2):103–116

    Google Scholar 

  • Calatayud V, Sanz MJ, Aptroot A (2001) Lichenopyrenis galligena (Pleomassariaceae), a new genus of gall-forming lichenicolous fungi on Leptochidium. Mycol Res 105(5):634–637

    Google Scholar 

  • Câmara MPS, Palm ME, van Berkum P, O’Neill NR (2002) Molecular phylogeny of Leptosphaeria and Phaeosphaeria. Mycologia 94:630–640

    PubMed  Google Scholar 

  • Câmara MP, Ramaley AW, Castlebury LA, Palm ME (2003) Neophaeosphaeria and Phaeosphaeriopsis, segregates of Paraphaeosphaeria. Mycol Res 107:516–522

    PubMed  Google Scholar 

  • Campbell J, Ferrer A, Raja HA, Sivichai S, Shearer CA (2007) Phylogenetic relationships among taxa in the Jahnulales inferred from 18S and 28S nuclear ribosomal DNA sequences. Can J Bot 85:873–882

    CAS  Google Scholar 

  • Cannon PF, Kirk PM (2007) Fungal families of the world. CABI Bioscience, Wallingford

    Google Scholar 

  • Carnegie AJ, Pegg GS, White D, Burgess TI (2011) Species within Mycosphaerellaceae and Teratosphaeriaceae from eucalypts in eastern Australia. Australas Plant Pathol 40:366–384

    Google Scholar 

  • Castlebury L, Crane J, Huhndorf S (1995) A new species of Rhytidenglerula from Everglades National Park, Florida. Mycotaxon 54:461–463

    Google Scholar 

  • Cesati V, de Notaris G (1863) Schema di classificazione deglesferiacei italici aschigeri piu’ o meno appartenenti al genere Sphaeria nell’antico significato attribuitoglide Persono. Comm Soc crittog Ital 1:177–420

    Google Scholar 

  • Chatmala IR, Valyase R, Tanticharoen M (2002) Anamorph/teleomorph connections of marine Ascomycota. In: Hyde KD (ed) Fungi in marine environments. Fungal Diversity Press, Hong Kong, pp 59–68

    Google Scholar 

  • Chaverri P, Gazis RO (2010) Perisporiopsis lateritia, a new species on decaying leaves of Hevea spp. from the Amazon basin in Peru. Mycotaxon 113:163–169

    Google Scholar 

  • Chaverri P, Liu M, Hodge KT (2008) A monograph of the entomopathogenic genera Hypocrella, Moelleriella, and Samuelsia gen. nov. (Ascomycota, Hypocreales, Clavicipitaceae), and their Aschersonia–like anamorphs in the Neotropics. Stud Mycol 60:1–66

    CAS  PubMed Central  PubMed  Google Scholar 

  • Checa J, Shoemaker RA, Umaña L (2007) Some new hysteriaceous fungi from Costa Rica. Mycologia 99:285–290

    CAS  PubMed  Google Scholar 

  • Cheewangkoon R, Groenewald JZ, Summerell BA, Hyde KD, To-anun C, Crous PW (2010) Myrtaceae, a cache of fungal biodiversity. Persoonia 23:55–85

    Google Scholar 

  • Chesters CGC, Bell A (1970) Studies in the Lophiostomataceae Sacc. Mycol Pap 120:1–55

    Google Scholar 

  • Chevallier FF (1826) Flore générale des environs de Paris, vol I. Ferra Librairie-Editeur, Paris

    Google Scholar 

  • Chilvers MI, Rogers JD, Dugan FM, Stewart JE, Chen W, Peever TB (2009) Didymella pisi sp. nov., the teleomorph of Ascochyta pisi. Mycol Res 113:391–400

    Google Scholar 

  • Choisy M (1955) Systematique des Roccellaceae, famille de lichens ascomycètes ascoloculaires. Bull Trimest Soc Mycol Fr 71(4):312–324

    Google Scholar 

  • Chomnunti P, Schoch CL, Aguirre-Hudson B, KoKo TW, Hongsanan S, Jones EBG, Kodsub R, Chukeatirote E, Bahkali AH, Hyde KD (2011) Capnodiaceae. Fungal Divers 51:103–134

    PubMed Central  PubMed  Google Scholar 

  • Chung KR (2011) Elsinoë fawcettii and Elsinoë australis: the fungal pathogens causing citrus scab. Mol Plant Pathol 12:123–135

  • Ciferri R, Tomaselli R (1953) Tentative mycolichenes classification. Atti dell’Istituto Botanico della Università e Laboratorio Crittogamico di Pavia Ser. 5 10(1):25–84

  • Ciferri R, Batista AC, Campos CA (1956) Taxonomy of Piedraia hortaiand systematic position of the Piedraiaceae family. Publções Inst Micol Recife 45:1–9

    Google Scholar 

  • Clements FE, Shear CL (1931) Genera of fungi, edn 2. i–vii, 58 plates. H.W. Wilson Company, USA, New York, p 496

  • Cole MS, Hawksworth DL (2004) Lichenoconium christiansenii sp. nov. from Nodobryoriaabbreviata (Parmeliaceae) in the Pacific Northwest, with a key to the known lichenicolous species. Lichenologist 36:1–6

    Google Scholar 

  • Conde BD, Pitkethley RN, Smith ESC, Kulkarni VJ, Thiagalingam K, Ulyatt LL, Connelly ML, Hamilton DA (1997) Disease notes or new records: identification of mango scab caused by Elsinoё mangiferae in Australia. Australas Plant Pathol 26:131

    Google Scholar 

  • Cooke WB (1983) Coniothyriaceae. Rev Biol (Lisbon) 12:289

  • Cooke MC, Hawksworth DL (1970) A preliminary list of families proposed for the fungi. Mycol Pap 121:1–86

    Google Scholar 

  • Coppins BJ (1988) Notes on the genus Arthopyrenia in the British Isles. Lichenologist 20:305–325

    Google Scholar 

  • Coppins BJ (2002) Checklist of lichens of Great Britain and Ireland. British Lichen Society, p 87

  • Coppins B, Kondratyuk SY (1995) Stygiomyces and Pseudonitschkia: two new genera of lichenicolous fungi. Edinb J Bot 52:229–236

    Google Scholar 

  • Corda ACJ (1838) Patellariaceae in Icones Fungorum hucusque Cognitorum 2:1–43

  • Corda ACJ (1842) Abbildungen der Pilze und Schwaemme. Icones Fungorum, Hucusque Cognitorum 5:34

  • Corlett M (1981) A taxonomic survey of some species of Didymella and Didymella–like species. Can J Bot 59:2016–2042

    Google Scholar 

  • Cortinas MN, Koch N, Thain J, Wingfield BD, Wingfield MJ (2004) First record of the Eucalyptus stem canker pathogen, Coniothyrium zuluense from Hawaii. Australas Plant Pathol 33:309–312

    Google Scholar 

  • Cortinas MN, Crous PW, Wingfield BD, Wingfield MJ (2006) Multi–gene phylogenies and phenotypic characters distinguish two species within the Colletogloeopsis zuluensis complex associated with Eucalyptus stem cankers. Stud Mycol 55:133–146

  • Crane JL (1971) Illinois fungi. 1. Chaetosticta. Can J Bot 49:31–34

  • Crane JL, Shearer CA (1991) A nomenclator of Leptosphaeria V. Cesati & G. de Notaris (Mycota, Ascomycotina, Loculoascomycetes). Bull Illinois State Nat Hist Surv 34:1–355

    Google Scholar 

  • Crivelli PG (1983) Über die heterogene Ascomycetengattung Pleospora Rabh.: Vorschlag für eine Aufteilung. Abh. Eidgenössischen Technischen Hochschule Zürich 7318: 213 pp

  • Crous PW (1998) Mycosphaerella spp. and their anamorphs associated with leaf spot diseases of Eucalyptus. Mycol Memories 21:1–170

    Google Scholar 

  • Crous PW, Braun U (2003) Mycosphaerella and its anamorphs.1. Names published in Cercospora, Passalora. CBS Biodivers Ser 1:1–571

    Google Scholar 

  • Crous PW, Kendrick WB (1994) Arnaudiella eucalyptorum sp. nov. (Dothideales, Ascomycetes) and its hyphomycetous anamorph. Can J Bot 72:59–64

    Google Scholar 

  • Crous PW, Aptroot A, Kang JC, Braun U, Wingfield MJ (2000) The genus Mycosphaerella and its anamorphs. Stud Mycol 45:107–121

    Google Scholar 

  • Crous PW, Kang JC, Braun U (2001) A phylogenetic redefinition of anamorph genera in Mycosphaerella based on ITS rDNA sequence and morphology. Mycologia 93:1081–1101

    CAS  Google Scholar 

  • Crous PW, Groenewald JZ, Aptroot A, Braun U, Xavier M, Carlier J (2003a) Integrating morphological and molecular data sets in Mycosphaerella, with specific reference to species occurring on Musa. In: Jacome L, Lepoivre P, Marin D, Ortiz R, Romero R, Escalant JV (eds) Mycosphaerella leaf spot diseases of bananas: present status and outlook. Proceedings of the Second International Workshop on Mycosphaerella leaf spot diseases of bananas, 20–23 May 2002, San José, Costa Rica. INIBAP. pp 43–57

  • Crous PW, Groenewald JZ, Gams W (2003b) Eyespot of cereals revisited: ITS phylogeny reveals new species relationships. Eur J Plant Pathol 109:841–850

    CAS  Google Scholar 

  • Crous PW, Groenewald JZ, Wingfield MJ, Aptroot A (2003c) The value of ascospore septation in separating Mycosphaerella from Sphaerulina in the Dothideales: a Saccardoan myth? Sydowia 55:136–152

    Google Scholar 

  • Crous PW, Groenewald JZ, Mansilla JP, Hunter GC, Wingfield MJ (2004) Phylogenetic reassessment of Mycosphaerella spp. and their anamorphs occurring on Eucalyptus. Stud Mycol 50:195–214

    Google Scholar 

  • Crous PW, Slippers B, Wingfield MJ, Rheeder J, Marasas WFO, Philips AJL, Alves A, Burgess TI, Barber PA, Groenewald JZ (2006) Phylogenetic lineages in the Botryosphaeriaceae. Stud Mycol 55:235–253

    PubMed Central  PubMed  Google Scholar 

  • Crous PW, Braun U, Groenewald JZ (2007a) Mycosphaerella is polyphyletic. Stud Mycol 58:1–3

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Braun U, Schubert K, Groenewald JZ (2007b) Delimiting Cladosporium from morphologically similar genera. Stud Mycol 58:33–56

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Schubert K, Braun U, de Hoog GS, Hocking AD, Shin HD, Groenewald JZ (2007c) Opportunistic, human-pathogenic species in the Herpotrichiellaceae are phenotypically similar to saprobic or phytopathogenic species in the Venturiaceae. Stud Mycol 58:185–217

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Braun U, Wingfield MJ, Wood AR, Shin HD, Summerell BA, Alfenas AC, Cumagun CJR, Groenewald JZ (2009a) Phylogeny and taxonomy of obscure genera of microfungi. Persoonia 22:139–161

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ (2009b) Phylogenetic lineages in the Capnodiales. Stud Mycol 64:17–47

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Summerell BA, Carnegie AJ, Wingfield MJ, Groenewald JZ (2009c) Novel species of Mycosphaerellaceae and Teratosphaeriaceae. Persoonia 23:119–145

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Summerell BA, Carnegie AJ, Wingfield MJ, Hunter GC, Burgess TI, Andjic V, Barber PA, Groenewald JZ (2009d) Unravelling Mycosphaerella: do you believe in genera? Persoonia 23:99–118

    CAS  PubMed Central  PubMed  Google Scholar 

  • Crous PW, Tanaka K, Summerell BA, Groenewald JZ (2011) Additions to the Mycosphaerella complex. IMA Fungus 2:49–64

    PubMed Central  PubMed  Google Scholar 

  • Crous PW, Summerell BA, Shivas RG, Burgess TI, Decock CA (2012) Fungal Planet description sheets: 107–127 Persoonia 28:138–182

    Google Scholar 

  • Crous PW, Braun U, Hunter GC, Wingfield MJ, Verkley GJM, Shin HD, Nakashima C, Groenewald JZ (2013) Phylogenetic lineages in Pseudocercospora. Stud Mycol 75:37–114

    CAS  PubMed Central  PubMed  Google Scholar 

  • Cunnell GJ (1961) Stagonospora macropycnidia sp. nov. Trans Br Mycol Soc 55:87–90

    Google Scholar 

  • Cuomo V, Vanzanella F, Fresi E, Cinelli F, Mazzella L (1985) Fungal flora of Posidonia oceanica and its ecological significance. Trans Br Mycol Soc 84:35–40

    Google Scholar 

  • Currah RS (1985) Taxonomy of the Onygenales: Arthrodermataceae, Gymnoascaceae, Myxotrichaceae and Onygenaceae. Mycotaxon 24:103–105

    Google Scholar 

  • Currah RS (1994) Peridial morphology and evolution in the Prototunicatea scomycetes. In: Hawksworth DL (ed) Ascomycete systematics: problems and perspectives in the nineties. Plenum Press, New York, pp 281–293

    Google Scholar 

  • Cybertruffle (2013) http://www.cybertruffle.org.uk/spegazzini/eng/002103a.html

  • Dai DQ, Jayarama Bhat D, Liu JK, Chukeatirote E, Zhao RL, Hyde KD (2012) Bambusicola, a new genus from bamboo with asexual and sexual morphs. Cryptog Mycolog 33:363–379

    Google Scholar 

  • Damm U, Verkley GJM, Crous PW, Fourie PH, Haegi A, Riccioni L (2008) Novel Paraconiothyrium species on stone fruit trees and other woody hosts. Persoonia 20:9–17

    CAS  PubMed Central  PubMed  Google Scholar 

  • Danilo BP Jr, Honorato J, Nicoli A Jr, Hora BT, Braganca CAD, Pereira OL (2012) Phylogenetic placement of the genus Anhellia and the description of A. nectandrae sp. nov. Mycologia 104:1291–1298

    Google Scholar 

  • Darker GD (1963) A new genus of the Lophiaceae. Can J Bot 41:1383–1388

    Google Scholar 

  • David JC, Hawksworth DL (1991) Validation of six family names of lichenized ascomycetes. Systema Ascomycetum 10:13–16

    Google Scholar 

  • de Gruyter JD, Aveskamp MM, Woudenberg JHC, Verkley GJM, Groenewald JZ, Crous PW (2009) Molecular phylogeny of Phoma and allied anamorph genera: towards a reclassification of the Phoma complex. Mycol Res 113:508–519

    PubMed  Google Scholar 

  • de Gruyter JD, Woudenberg JH, Aveskamp MM, Verkley GJ, Groenewald JZ, Crous PW (2010) Systematic reappraisal of species in Phoma section Paraphoma, Pyrenochaeta and Pleurophoma. Mycologia 102:1066–1081

    PubMed  Google Scholar 

  • de Gruyter JD, Woudenberg JHC, Aveskamp AA, Verkley GJM, Groenewald JZ, Crous PW (2012) Redisposition of Phoma-like anamorphs in Pleosporales. Stud Mycol 75:1–36

    PubMed Central  Google Scholar 

  • de Hoog GS, Oorschot CAN van, Hijwegen T (1983) Taxonomy of the Dactylaria complex. II. Dissoconium gen. nov. and Cordana preuss. Proceedings of the Koninklijke Nederlandse Akademie van Wetenschappen, Series C 86:197–206

  • de Hoog GS, Guarro J, Gené J, Figueras MJ (2000) Atlas of Clinical Fungi. 2nd edn. Centraalbureau voor Schimmelcultures, Utrecht, Netherlands, and Universitat Rovira I Virgili, Reus, Spain

  • de Liyanage AS, Jayasinghe CK, Liyanage NIS, Jayaratne R (1986) Corynespora leaf spot disease of rubber (Hevea brasiliensis) a new record. J Rubber Res Inst Sri Lanka 65:47–50

    Google Scholar 

  • de Notaris G (1845) Micromycetes Italici novi vel minus cogniti. V Mem R Acc Sci Torino 2(10):333–350

    Google Scholar 

  • Deighton FC (1976) Studies on Cercospora and allied genera. VI. Pseudocercospora Speg., Pantospora Cif. and Cercoseptoria Petr. Mycol Pap 140:1–168

    Google Scholar 

  • Del Prado R, Schmitt I, Kautz S, Palice Z, Lücking R, Lumbsch HT (2006) Molecular data place Trypetheliaceae in Dothideomycetes. Mycol Res 110:511–520

    PubMed  Google Scholar 

  • Dennis RWG (1968) British ascomycetes, 2nd edn. J. Cramer, Vaduz

    Google Scholar 

  • Dennis RWG (1978) British ascomycetes, 3rd edn. J. Cramer, Vaduz

    Google Scholar 

  • Desmazières JBHJ (1841) Huitième notice sur quelques plantes cryptogames, la plupart inédites, récemment découvertes en France. Ann Sci Nat Bot 15:129–146

    Google Scholar 

  • Desmazières JBHJ (1849) Dix–septième notice sur les plantes cryptogames récemment découvertes en France. Ann Sci Nat Bot Ser 3(11):360

    Google Scholar 

  • Dixon LJ, Schlub RL, Pernezny K, Datnoff LE (2009) Host specialization and phylogenetic diversity of Corynespora cassiicola. Phytopathology 99:1015–1027

    CAS  PubMed  Google Scholar 

  • Döbbeler P (1984) Symbiosen zwischen Gallertalgen und Gallertpilzen der Gattung Epigloea (Ascomycetes). In: Hertel H, Oberwinkler F (eds) Beitrage zur Lichenologie. Festscrift J. Poelt. Beiheft zur Nova Hedwigia 79. J. Cramer, Vaduz, pp 203–239

  • Döbbeler P (1994) Epigloea urosperma (Ascomycetes) ein neuer Flechtenparasit. Sendtnera 2:277–282

    Google Scholar 

  • Doidge EM (1942) South African Microthyriaceae. Bothalia 4:273–344

    Google Scholar 

  • Doilom M, Liu JK, Jaklitsch WM, Ariyawansa H, Wijayawardene NN, Chukeatirote E, Zhang M, McKenzie EHC, Geml J, Voglmayr H, Hyde KD (2013) An outline of the family Cucurbitariaceae. Sydowia 65(1):167–192

    Google Scholar 

  • Dong J, Chen W, Crane JL (1998) Phylogenetic studies of the Leptosphaeriaceae, Pleosporaceae and some other loculoascomycetes based on nuclear ribosomal DNA sequences. Mycol Res 102(2):151–156

    CAS  Google Scholar 

  • Duby JE (1862) Memoire sur la tribu des Hysterinees de la famille des Hypoxylees (Pyrenomycetes). Mem Soc Phys Hist Nat Genève 16:15–70

    Google Scholar 

  • Dugan JE, Jaramillo E, Hubbard DM, Contreras H, Duarte C (2004) Competitive interactions in macroinfaunal animals of exposed sandy beaches. Oecologia 139:630–640

    PubMed  Google Scholar 

  • Durieu C, Montagne JFC (1956) Sylloge genereum Specierumque Cryptoamarum. Bailliére et Fils, Paris, p 229

    Google Scholar 

  • Durieux M (1963) Comment. Soc Crittogam Ital 1:224

    Google Scholar 

  • Eaton RA, Jones EBG (1971) New fungi on timber from water-cooling towers. Nova Hedwigia 19(779):783

    Google Scholar 

  • Ellis MB (1949) Tetraploa. Trans Br Mycol Soc 32:246–251

    Google Scholar 

  • Ellis MB (1971) Dematiaceous hyphomycetes. Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Ellis JP (1976) British Microthyrium species and similar fungi. Trans Br Mycol Soc 67(3):381–394

    Google Scholar 

  • Ellis JP (1980) The genus Morenoina in Britain. Trans Br Mycol Soc 74:297–307

    Google Scholar 

  • Ellis JB, Everhart BM (1892) The North American pyrenomycetes. Newfield, NJ

    Google Scholar 

  • Eriksson OE (1967) On graminicolous pyrenomycetes from Fennoscandia. I, II, III. Ark Bot Ser 26:339–466

    Google Scholar 

  • Eriksson OE (1981) The families of bitunicate ascomycetes. Nord J Bot 1(6):800

    Google Scholar 

  • Eriksson OE (1982) Outline of the ascomycetes. Mycotaxon 15:203–248

    Google Scholar 

  • Eriksson OE (1994) Problems in the classification of fissitunicate ascomycetes. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. NATO ASI, vol 269. Plenum Press, New York and London, pp 341–345

    Google Scholar 

  • Eriksson OE (2005) Outline of Ascomycota, The present classification contains all accepted genera and higher taxa above the generic level in phylum Ascomycota. Myconet 11:1–113

    Google Scholar 

  • Eriksson OE (2006) Outline of Ascomycota. Myconet 12:1–88

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1986a) Notes on ascomycete systematics. Nos. 1–224. Syst Ascomycetum 5:113–174

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1986b) Outline of the ascomycetes. Syst Ascomycetum 5:185–324

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1987) Outline of the ascomycetes. Syst Ascomycetum 6:259–337

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1991) Outline of the Ascomycetes 1990. Systema Ascomycetum 1–4 (1982–1985) 9: 39–271

  • Eriksson OE, Hawksworth DL (1992) Notes on ascomycete systematics 1294–1417. Syst Ascomycetum 11:49–82

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1993) Notes on ascomycete systematics – Nos 1418–1529. Syst Ascomycetum 11:163–194

    Google Scholar 

  • Eriksson OE, Hawksworth DL (2003) Saccharicola, a new genus for two Leptosphaeria species on sugar cane. Mycologia 95:426–433

    PubMed  Google Scholar 

  • Eriksson OE, Yue JZ (1990) Notes on bambusicolous pyrenomycetes. Mycotaxon 38:201–220

    Google Scholar 

  • Eriksson OE, Baral HO, Currah RS, Hansen K, Kurtzman CP, Rambold G, Laessøe T (2004) Outline of Ascomycota. Myconet 10:1–99

    Google Scholar 

  • Ertz D, Lawrey JD, Common RS, Diederich P (2013) Molecular data resolve a new order of Arthoniomycetes sister to the primarily lichenized Arthoniales and composed of black yeasts, lichenicolous and rock-inhabiting species. Fungal Diversity 1–25

  • Etayo J (2002) Catálogo de líquenes y hongos liquenícolas del Parque Natural de Bértiz (Navarra, España). Bull Soc Linnéenne Provence 53:155–171

    Google Scholar 

  • Etayo J, Sancho LG (2008) Hongos liquenícolas del sur de Sudamérica, especialmente de Isla Navarino (Chile). Bibl Lichenologica 98:1–302

    Google Scholar 

  • Etayo J, Van den Boom PPG (2006) Some lichenicolous fungi from Guatemala, with the description of a new species. Herzogia 19:191–197

    Google Scholar 

  • Fallah PM, Shearer CA (2001) Freshwater ascomycetes: new or noteworthy species from north temperate lakes in Wisconsin. Mycologia 93:566–602

    Google Scholar 

  • Farr ML (1979) The didymosporous dimeriaceous fungi described on Asteraceae. Mycologia 71:243–803

    Google Scholar 

  • Farr DF, Rossman AY (2012) Fungal databases, systematic mycology and microbiology laboratory, ARS, USDA. http://nt.ars-grin.gov/fungaldatabases/Retrieved 25 October 2011

  • Farr DF, Bills GF, Chamuris GP, Rossman AY (1989) Fungi on plants and plant products in the United States. APS Press, St. Paul

    Google Scholar 

  • Faull JL, Olejnik I, Ingrouille M, Reynolds D (2002) A reassessment of the taxonomy of some tropical sooty moulds. Tropical mycology volume 2. Micromycetes. CABI, UK, pp 33–40

    Google Scholar 

  • Ferrer A, Miller AN, Shearer CA (2011) Minutisphaera and Natipusilla: two new genera of freshwater Dothideomycetes. Mycologia 103:411–423

    PubMed  Google Scholar 

  • Fink B (1910) The lichens of Minnesota. Contributions from the U.S. National Museum. 14:1–269

  • Fink B (1913) The nature and classification of lichens II. The lichen and its algal host. Mycologia 5:111

    Google Scholar 

  • Fisher PJ, Webster J (1992) A Trematosphaeria endophyte from rice roots and its Zalerion anamorph. Nova Hedwigia 54:77–81

    Google Scholar 

  • Fonseca O, Leão AE d A (1928) Sobre os cogumelos da piedra brazileira. Mem Inst Oswaldo Cruz 21(suppl 4):124–127

    Google Scholar 

  • Foucard T (1992) Notes on the corticolous Arthopyrenia–species in Sweden. Graphis Scripta 4:49–60

    Google Scholar 

  • Fries EM (1818) Observationes mycologicae. Gerh. Bonnier, Copenhagen 2:347–351

  • Fries EM (1823) Systema mycologicum, vol.2, section II,. 620 pages Gryphiswaldiae

  • Fuckel L (1870) Beiträge zur Kenntniss der Rheinischen Pilze. Jahrbücher Nassauischen Vereins Naturkunde 23–24:1–459

    Google Scholar 

  • Fuckel KWGL (1871) Symbolae mycologicae. Beiträgezur Kenntniss der Rheinischen Pilze. Erster Nachtrag. Jahrbücher Nassauischen Vereinsfür Naturkunde 25–26:25

    Google Scholar 

  • Gams W (1999) Report of the committee for fungi: 8. Taxon 48:807–810

    Google Scholar 

  • Gamundí IJ, Spinedi MA (1985) Phaneromyces Speg. & Hariot, a discomycetous genus of critical taxonomic position. Sydowia 38:106–113

    Google Scholar 

  • Gaumann EA (1949) Die Pilze, Grundzu¨ge ihrer Entwicklungsgeschichte und Morphologie. Birkhä user, Basel

    Google Scholar 

  • George M (1895) British fungus–flora. A classified text–book of mycology. G. Bell and Sons, London

    Google Scholar 

  • Glienke C, Pereira OL, Stringari D, Fabris J, Kava-Cordeiro V, Galli-Terasawa L, Cunnington J, Shivas RG, Groenewald JZ, Crous PW (2011) Endophytic and pathogenic Phyllosticta species, with reference to those associated with Citrus Black Spot. Persoonia 26:47–56

    CAS  PubMed Central  PubMed  Google Scholar 

  • Goebel F, Kunze G (1827) Pharmazeutische Waarenkunde. Eisenach Gonidien. Österreichische botanische Zeitschrift 40:323–328

    Google Scholar 

  • Gordon CC, Shaw CG (1960) A new genus of the Meliolaceae on the roots of Solanum species. Mycologia 52:331

    Google Scholar 

  • Goree H (1974) Glyphium in western Canada and United States. Can J Bot 52:1265–1269

    Google Scholar 

  • Gray SF (1821) A natural arrangment of British plants vol.1, p 519

  • Greville RK (1824) Flora Edinensis: or a description of plants growing near Edinburgh, arranged according to the linnean system. i–lxxxi, 4 tabs. Blackwood, Edinburgh, p 478

    Google Scholar 

  • Greville RK (1825a) Scottish cryptogamic flora or coloured figures and descriptions of cryptogamic plants found in Scotland and belonging chiefly to the order fungi and intended to serve as a continuation of english botany 3: tabs. Maclachnan, Edinburgh, pp 121–180

    Google Scholar 

  • Greville RK (1825b, publ. 1826) Scottish Cryptogamic Flora 4 (37–48): plates 181–240. Scotland, Edinburgh

  • Griffiths D (1901) The North American Sordariaceae. Mem Torrey Bot Club 11:1–134

    Google Scholar 

  • Groenewald JZ, Nakashima C, Nishikawa J, Shin HD, Park JH, Jama AN, Groenewald M, Braun U, Crous PW (2012) Species concepts in Cercospora: spotting the weeds among the roses. Stud Mycol 75:115–170

    Google Scholar 

  • Groenewald JZ, Nakashima C, Nishikawa J, Shin HD, Park JH, Jama AN, Groenewald M, Braun U, Crous PW (2013) Species concepts in Cercospora: spotting the weeds among the roses. Stud Mycol 75:115–170

    CAS  PubMed Central  PubMed  Google Scholar 

  • Groenhart P (1951) Malaysian lichens III. Cyanoporina Groenh., an interesting lichen from Java. Reinwardtia 1:197–198

    Google Scholar 

  • Grube M (1993) Über metachromatisches Färbeverhalten bei einigen Arten der Sammelgattung Arthopyrenia, mit weiteren Beispielen aus ähnlichen Gattungen (Ascomycetes, Arthopyreniaceae). Nova Hedwigia 57:473–482

    Google Scholar 

  • Hafellner J (1979) Kurschia. Revision einer Sammelgattung an der Grenze von lichenisierten und nichtlichenisierten Ascomyceten. Beih Nova Hedwigia 62:1–248

    Google Scholar 

  • Hafellner J (1982) Studien uber lichenicole Pilze und Flechten II. Lichenostigma maureri gen. et spec. nov., ein in den Ostalpen haufiger lichenicoler Pilz (Ascomycetes, Arthoniales). Herzogia 6:299–308

    Google Scholar 

  • Halici MG, Hawksworth DL (2008) Two new species of Dacampia (Ascomycota, Dacampiaceae), with a key to and synopsis of the known species of the genus. Fungal Divers 28:49–54

    Google Scholar 

  • Hall T (2004) BioEdit v. 7.0.1. Department of Microbiology, North Carolina State University. Available at www.mbio.ncsu.edu/BioEdit/bioedit.html

  • Hambleton S, Egger KN, Currah RS (1998) The genus Oidiodendron: species delimitation and phylogenetic relationship based on nuclear ribosomal DNA analysis. Mycologia 90:854–869

    CAS  Google Scholar 

  • Hambleton S, Tsuneda A, Currah RS (2003) Comparative morphology and phylogenetic placement of two microsclerotial black fungi from Sphagnum. Mycologia 95:959–975

    CAS  PubMed  Google Scholar 

  • Hanlin RT (1989) Illustrated genera of ascomycetes. APS Press. The American Phytopathological Society, St. Paul

    Google Scholar 

  • Hansford GC (1945) Contributions towards the fungus flora of Uganda. VII. New records and revisions. Proc Linnean Soc London 157:37–38

    Google Scholar 

  • Hansford GC (1946) The foliicolous ascomycetes, their parasites and associated fungi. Mycol Pap 15:1–240

    Google Scholar 

  • Harris RC (1973) The corticoloios pyrenolichens of the Great Lakes region. Mich Bot 12:3–68

    Google Scholar 

  • Harris RC (1975) A taxonomic revision of the genus Arthopyrenia Massal. s. lat. (Ascomycetes) in North America. Ph.D. Thesis, Michigan State University, USA, p 288

  • Harris R (1984) The family Trypetheliaceae (Loculoascomycetes: lichenized Melanommatales) in Amazonian Brazil. Suppl Acta Amazônica 14:55–80

    Google Scholar 

  • Harris RC (1990) Some Florida lichens. Publ. by the Author, Bronx

    Google Scholar 

  • Harris RC (1995) More Florida lichens. Including the 10c tour of the pyrenolichens. Author, Bronx

    Google Scholar 

  • Hatakeyama S, Tanaka K, Harada Y (2005) Bambusicolous fungi in Japan (5): three species of Tetraploa. Mycoscience 46:196–200

    Google Scholar 

  • Hausmann S, Lotter AF, van Leeuwen JFN, Ohlendorf C, Lemcke G, Grönlund R, Sturm M (2002) Interactions of climate and land use documented in the varved sediments of Seebergsee in the Swiss Alps. Holocene 12:279–289

    Google Scholar 

  • Hawksworth DL (1977) Taxonomic and biological observations on the genus Lichenoconium (Sphaeropsidales). Persoonia 9:159–198

    Google Scholar 

  • Hawksworth DL (1979) Ascospore sculpturing and generic concepts in the Testudinaceae (syn. Zopfiaceae). Can J Bot 57:91–99

    Google Scholar 

  • Hawksworth DL (1981) Lichenothelia, a new genus for the Microthelia aterrima group. Lichenologist 13:141–153

    Google Scholar 

  • Hawksworth DL (1985a) A redisposition of the species referred to the ascomycete genus Microthelia. Bulletin of the British Museum (Natural History). Botany 14:43–181

    Google Scholar 

  • Hawksworth DL (1985b) Kirschsteiniothelia a new genus for the Microthelia incrustans–group (Dothideales). Bot J Linn Soc 91:181–202

    Google Scholar 

  • Hawksworth DL (2012) Managing and coping with names of pleomorphic fungi in a period of transition. Mycosphere 3:143–155

    Google Scholar 

  • Hawksworth DL, Boise JR (1985, publ. 1986) Some additional species of Astrosphaeriella, with a key to the members of the genus. Sydowia 38:114–124

    Google Scholar 

  • Hawksworth DL, Booth C (1974) A revision of the genus Zopfia Rabenh. Mycol Pap 135:1–38

    Google Scholar 

  • Hawksworth DL, David JC (1989) Proposals for nomina conservanda and rejicienda for ascomycete names (lichenized and nonlichenized). Taxon 38:493–499

    Google Scholar 

  • Hawksworth DL, Diederich P (1988) A synopsis of the genus Polycoccum (Dothideales), with a key to accepted species. Trans Br Mycol Soc 90:293–312

    Google Scholar 

  • Hawksworth DL, Eriksson OE (1986) The names of accepted orders of ascomycetes. Syst Ascomycetum 5:175–184

    Google Scholar 

  • Hawksworth DL, Eriksson OE (1988) Proposals to conserve 11 family names in the Ascomycotina (Fungi). Taxon 37:190–193

    Google Scholar 

  • Hawksworth DL, Mcmanus PM (1989) Lichen recolonization in London under conditions of rapidly falling sulphur dioxide levels, and the concept of zone skipping. Bot J Linn Soc 100:99–109

    Google Scholar 

  • Hawksworth DL, Kirk PM, Sutton BC, Pegler DN (1983) Ainsworth & Bisby’s dictionary of the fungi. Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Hawksworth DL, Kirk PM, Sutton BC, Pegler DN (1995) Ainsworth & Bisby’s dictionary of the fungi, 8th edn. CAB International, Wallingford

    Google Scholar 

  • Hawksworth DL, Crous PW, Redhead SA, Reynolds DR, Samson RA, Seifert KA, Taylor JW, Wingfield MJ et al. (2011) The Amsterdam declaration on fungal nomenclature. IMA Fungus 2: 105–112; Mycotaxon 116:491–500

    Google Scholar 

  • Hedrick J (1942) Some lichens from the American tropics collected by Wm. R. Taylor. Allan Hancock Pac Expeditions 3:183–187

    Google Scholar 

  • Hennings PC (1895) Fungi Goyazenses. Hedwigia 34:88–116

    Google Scholar 

  • Hennings PC (1900) Fungi japonica. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie. Pflanzengeogr 28:259–280

    Google Scholar 

  • Hennings PC (1904a) Einige neue Pilze aus Japan. Hedwigia 43:143–144

    Google Scholar 

  • Hennings P (1904b) Fungi Africae orientalis III. Bot Jahrb Syst Pflanzengesch Pflanzengeogr 34:39–57

    Google Scholar 

  • Hennings PC (1904c) Fungi fluminenses a cl. E. Ule collecti. Hedwigia 43:78–95

    Google Scholar 

  • Henssen A (1964) Was it Pyrenothrix nigra? Ber Deut Bot Ges 77:317–322

    Google Scholar 

  • Henssen A (1987) Lichenothelia, a genus of microfungi on rocks. In: Peveling E (ed) Progress and problems in lichenology in the eighties. Bibliotheca Lichenologica No.25. J. Cramer, Berlin-Stuttgart, pp 257–293

    Google Scholar 

  • Henssen A (1995) Studies on the biology and structure of Dacampia (Dothideales), a genus with lichenized and lichenicolous species. Cryptogam Bot 5:149–158

    Google Scholar 

  • Henssen A, Jahns HM (1973) Lichenes. Georg Thieme Verlag, Stuttgart

    Google Scholar 

  • Henssen A, Thor G (1994) Developmental morphology of the ‘Zwischengruppe’ between Ascohymeniales and Ascoloculares. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. NATO ASI series vol 269. Plenum Press, New York and London, pp 43–56

    Google Scholar 

  • Herrera-Campos ML, Huhndorf S, Lücking R (2005) The foliicolous lichen flora of Mexico IV: a new, foliicolous species of Pyrenothrix (Chaetothyriales, Pyrenothrichaceae). Mycologia 97:356–361

    Google Scholar 

  • Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Eriksson OE, Huhndorf S, James ST, Kirk PM, Lucking R, Lumbsch HT, Lutzoni F, Matheny PB, Mclaughlin DJ, Powell MJ, Redhed S, Schoch CL, Spatafora JF, Stalpers JA, Vilgalys R, Aime MC, Aptroot AA, Bauer R, Begerow D, Benny GL, Castelbury LA, Crous PW, Dai YC, Gams W, Geiser DM, Griffith GW, Gueidan C, Hawksworth DL, Hestmark G, Hosaka K, Humber RA, Hyde KD, Ironisde JE, Koljag U, Kurtzman CP, Larsson KH, Lichtwardt R, Longcore J, Miadlikowska J, Miller A, Moncalvo JM, Mozley-Standridge S, Oberwinkler F, Parmasto E, Reeb V, Rogers JD, Roux C, Ryvarden L, Sampaio JP, Schβler A, Sugiyama J, Thorn RG, Tibell L, Untereiner WA, Walker C, Wang Z, Weir A, Weiss M, White MM, Winka K, Yao YJ, Zhang N (2007) A higher–level phylogenetic classification of the fungi. Mycol Res 111:509–547

    PubMed  Google Scholar 

  • Hillis DM, Bull JJ (1993) An empirical test of bootstrapping as a method for assessing confidence in phylogenetic analysis. Syst Biol 42:182

    Google Scholar 

  • Hino I, Katumoto K (1965) Notes on bambusicolous fungi (1). J Japanese Bot 40:81–89

    Google Scholar 

  • Hirayama K, Tanaka K (2011) Taxonomic revision of Lophiostoma and Lophiotrema based on reevaluation of morphological characters and molecular analyses. Mycoscience 52:401–412

    Google Scholar 

  • Hirayama K, Tanaka K, Raja HA, Miller AN, Shearer CA (2010) A molecular phylogenetic assessment of Massarina ingoldiana sensu lato. Mycologia 102:729–746

    CAS  PubMed  Google Scholar 

  • Hodhod MS, Abdel-Wahab MA, Bahkali AHA, Hyde KD (2012) Amarenographium solium sp nov from Yanbu mangroves in the Kingdom of Saudi Arabia. Cryptogam Mycol 33(3):285–294

    Google Scholar 

  • Hofmann TA, Piepenbring M (2006) New records and host plants of fly–speck fungi from Panama. Fungal Divers 22:55–70

    Google Scholar 

  • Hofmann TA, Kirschner R, Piepenbring M (2010) Phylogenetic relationships and new records of Asterinaceae (Dothideomycetes) from Panama. Fungal Divers 43:39–53

    Google Scholar 

  • Höhn.ex Trotter, Sacc., D. Sacc. & Traverso [as ‘Schizothyrieae’] (1928) in Saccardo, Syll. fung. (Abellini) 24(2):1254

    Google Scholar 

  • Hohnel FXR (1907) Eumycetes et myxomycetes. Denskriften der Kaiserlichen Akademie der Wissenschaften 1(118):813–904

    Google Scholar 

  • Holm L, Holm K (1977) A study of Leptopeltidaceae. Bot Notiser 130:215–229

    Google Scholar 

  • Holm L, Holm K (1988) Studies in the Lophiostmataceae with emphasis on the Swedish species. Symbolae Botanicae Upsalienses 28:1–50

    Google Scholar 

  • Hooker JD (1847) The Botany of the Antarktic Voyage of H.M. Discovery Ships Erebus and Terror in the Years 1839-43 under the Command of Captain Sir James Clark Ross. I. Flora Antarctica Part 1.- London

  • Hooker JD, Harvey WH (1847) Algae Antarctiae: being characters and descriptions of the hitherto unpublished species of Algae, discovered in Lord Auckland’s Group, Campbell’s Islands, Kerguelen’s Land, Falkland Islands, Cape Horn and other southern circumpolar regions, during the voyage of H.M. discovery ships “Erebus” and “Terror”. London J Bot 4:249–276, 293–298

    Google Scholar 

  • Hosagoudar VB (2003) Studies on Foliicoclous fungi–XIII a new genus and a new species. Zoos Print J 18:1159–1162

    Google Scholar 

  • Hosagoudar VB (2004) Studies on Foliicolous fungi. Econ Taxon Bot 28:187–195

    Google Scholar 

  • Hosagoudar VB (2006) Additions to the fungi of Kerala. Zoos’ Print J 21(8):2356–2371

    Google Scholar 

  • Hosagoudar VB (2011) The genus Schiffnerula in India. Plant Pathol Quar 1:131–204

    Google Scholar 

  • Hosagoudar VB (2012) Asterinales of India. Mycosphere 2(5):617–852

    Google Scholar 

  • Hosagoudar VB (2013) My contribution to the fungal knowledge of India. J Threatened Taxa 5(8):4129–4348

    Google Scholar 

  • Hosagoudar VB, Biju CK, Abraham TK (2004) Additions to Asterinaceae. Indian Phytopathol 57:114–116

    Google Scholar 

  • Hosagoudar VB, Sabeena A, Kamarudeen M (2011a) A new species of the genus Englerula from India. Mycosphere 2:215–217

    Google Scholar 

  • Hosagoudar VB, Thimmaiah C, Jayashankara M (2011b) Schiffnerulaceous fungi of Kodagu, Karnataka, India. J Threatened Taxa 3:2268–2271

    Google Scholar 

  • Hu DM, Cai L, Chen H, Bahkali AH, Hyde KD (2010) Four new freshwater fungi associated with submerged wood from Southwest Asia. Sydowia 62:191–203

    Google Scholar 

  • Huelsenbeck JP, Ronquist F (2001) MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17:754–755

    CAS  PubMed  Google Scholar 

  • Hughes SJ (1953a) Conidiophores, conidia and classification. Can J Bot 31:577–659

    Google Scholar 

  • Hughes SJ (1953b) Fungi from the Gold Coast. II. Mycol Pap 50:1–104

    Google Scholar 

  • Hughes SJ (1965) New Zealand Fungi: 5. Trichothallus and Plokamidomyces states of Trichopeltheca. N Z J Bot 3:320–332

    Google Scholar 

  • Hughes SJ (1966) New Zealand Fungi 7. Capnocybe and Capnophialophora, new form genera of sooty moulds. N Z J Bot 4:333–353

    Google Scholar 

  • Hughes SJ (1968) Strigopodia. Can J Bot 46:1099–1107

    Google Scholar 

  • Hughes SJ (1972) New Zealand fungi 17. Pleomorphism in Euantennariaceae and Metacapnodiaceae, two new families of sooty moulds. N Z J Bot 10:225–242

    Google Scholar 

  • Hughes SJ (1974) New Zealand Fungi 22. Euantennaria with Antennatula and Hormisciomyces states. N Z J Bot 12(3):299–356

    Google Scholar 

  • Hughes SJ (1976) Sooty moulds. Mycologia 68:693–820

    Google Scholar 

  • Hughes SJ (1981) New Zealand Fungi 31. Capnobotrys, an anamorph of Metacapnodiaceae. N Z J Bot 19:193–226

    Google Scholar 

  • Hughes SJ (1993) Meliolina and its excluded species. Mycol. Pap. 166:176

  • Hughes SJ (2000) Antennulariella batistae n.sp. and its Capnodendron and Antennariella synanamorphs with notes on Capnodium capsuliferum. Can J Bot 78:1215–1226

    Google Scholar 

  • Hughes SJ (2003) Capnofrasera dendryphioides, a new genus and species of sooty moulds. N Z J Bot 41:139–146

    Google Scholar 

  • Hughes SJ (2007) Heteroconium and Pirozynskiella n. gen., with comments on conidium transseptation. Mycologia 99:628–638

    CAS  PubMed  Google Scholar 

  • Hughes SJ, Seifert KA (2012) Taxonomic and nomenclatural notes on Sooty mould names based on species mixtures: Hormiscium handelii and Torula lechleriana. Mycoscience 53:17–24

    Google Scholar 

  • Huhndorf SM (1992) Neotropical ascomycetes 2. Hypsostroma, a new genus from the Dominican Republic and Venezuela. Mycologia 84:750–758

    Google Scholar 

  • Huhndorf SM (1994) Neotropical Ascomycetes 5. Hypsostromataceae, a new family of Loculoascomycetes and Manglicola samuelsii, a new species from Guyana. Mycologia 86:266–269

    Google Scholar 

  • Huhndorf SM, Glawe DA (1990) Pycnidial development from ascospores of Fenestella princeps. Mycologia 82:541–548

    Google Scholar 

  • Huhndorf SM, Fernández FA, Miller AN, Lodge DJ (2003) Neotropical Ascomycetes 12. Mirannulata samuelsii gen. et sp. nov. and M. costaricensis sp. nov., new taxa from the Caribbean and elsewhere. Sydowia 55:172–180

    Google Scholar 

  • Hyde KD (1988) Studies on the tropical marine fungi of Brunei. Bot J Linn Soc 98:135–151

    Google Scholar 

  • Hyde KD (1991) A new amphisphaeriaceous fungus from intertidal fronds of Nypa fruticans. Trans Mycol Soc Jpn 32:265–271

    Google Scholar 

  • Hyde KD (1992b) Tropical Australian freshwater fungi 1. Aust Syst Bot 6:161–167

    Google Scholar 

  • Hyde KD (1992c) The genus Saccardoella from intertidal mangrove wood. Mycologia 84(5):803–810

    Google Scholar 

  • Hyde KD (1992d) Julella avicenniae (Borse) comb. nov. (Thelenellaceae) from intertidal mangrove wood and miscellaneous fungi from the NE coast of Queensland. Mycol Res 96:939–942

    Google Scholar 

  • Hyde KD (1995) The genus Massarina, with a description of M.eburnea and an annotated list of Massarina names. Mycol Res 99:291–296

    Google Scholar 

  • Hyde KD (1996) Fungi from palms. XXIV. The genus Bondiella. Mycotaxon 57:347–352

    Google Scholar 

  • Hyde KD (1997) The genus Roussoëlla, including two new species from palms in Cuyabeno, Ecuador. Mycol Res 101(5):609–616

    Google Scholar 

  • Hyde KD, Borse BD (1986) Marine fungi from Seychelles V. Biatriospora marina gen. et sp. nov. from mangrove wood. Mycotaxon 26:263–270

    Google Scholar 

  • Hyde KD, Borse BD (1991) Marine fungi from Seychelles VI. Massarina velatospora a new marine ascomycotina from mangrove wood. Mycotaxon 27:161–167

    Google Scholar 

  • Hyde KD, Jones EBG (1989) Intertidal mangrove fungi from Brunei. Lautospora gigantea gen. et sp. nov., a new loculoascomycete from prop roots of Rhizophora spp. Bot Mar 32:479–482

    Google Scholar 

  • Hyde KD, Steinke TS (1996) Two new species of Delitschia from submerged wood. Mycoscience 37:99–102

    Google Scholar 

  • Hyde KD, Eriksson OE, Yue J-Z (1996) Roussoëlla, an ascomycete genus of uncertain relationships with a Cytoplea anamorph. Mycol Res 100:1522–1528

    Google Scholar 

  • Hyde KD, Aptroot A, Fröhlich J, Taylor JE (2000) Fungi from palms. XLIII. Lophiostoma and Astrosphaeriella species with slit–like ostioles. Nova Hedwigia 70:143–160

    Google Scholar 

  • Hyde KD, McKenzie EHC, KoKo TW (2011) Towards incorporating anamorphic fungi in a natural classification checklist and notes for 2010. Mycosphere 2:1–88

    Google Scholar 

  • Hyun JW, Timmer LW, Lee SC, Yun SH, Ko SW, Kim KS (2001) Pathological characterization and molecular analysis of Elsinoё isolates causing scab diseases of Citrus in Jeju Island in Korea. Plant Dis 85:1013–1017

    CAS  Google Scholar 

  • Inácio CA, Cannon PF (2008) The genera of the Parmulariaceae. CBS biodiversity series vol 8. CBS Fungal Biodiversity Centre, Utrecht

    Google Scholar 

  • Inácio CA, Araúz K, Piepenbring M (2012) A new genus of Parmulariaceae from Panama. Mycol Prog 11–6

  • Inderbitzin P, Landvik S, Abdel-Wahab MA, Barbee ML (2001) Aliquandostipitaceae, a new family for two new tropical ascomycetes with unusually wide hyphae and dimorphic ascomata. Am J Bot 88:52–61

    PubMed  Google Scholar 

  • Index Fungorum (2013) http://www.indexfungorum.org/Names/Names.asp, Accession Date −02 November 2012

  • Jaag O, Thomas E (1934) Neue Untersuchungenüber die Flechte Epigloeabactrospora Zukal. Ber Schweizerischen Botanischen Ges 43:77–89

    Google Scholar 

  • Jackson S, Maxwell A, Neumeister-Kemp H, Dell B, Hardy G (2004) Infection, hyperparasitism and conidiogenesis of Mycosphaerella lateralis on Eucalyptus globulus in Western Australia. Australas Plant Pathol 33:49–53

    Google Scholar 

  • Janex-Favre MC (1971) Recherches sur l’ontogenie, l’organisation et les asques de quelques pyrenolichens. Rev Bryol Lichenol 37:421–469

    Google Scholar 

  • Jeng RS, Cain RF (1976) A new species of Eoterfezia from Mexico and Venezuela. Mycotaxon 3:387–390

    Google Scholar 

  • Jenkins AE, Ukkelberg HG (1935) Scab of Golden rod caused by Elsinoё. J Agric Res 51:515–525

    Google Scholar 

  • Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL (2009a) Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Divers 35:1–187

    Google Scholar 

  • Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL (2009b) Classification of marine origin and evolution of fundamental reproductive and ecological traits. Syst Biol 58:224–239

    Google Scholar 

  • Jones GE, Pang KL, Stanley SJ (2012) Fungi from marine algae. In: Jones EBG et al. (ed) Marine fungi and fungal-like organisms. Mar Freshw Botany 329–344

  • Kaiser WJ, Viruega JR, Peever TL, Trapero A (2008) First report of ascochyta blight outbreak of pea caused by Ascochyta pisi in Spain. Plant Dis 92:1365

    Google Scholar 

  • Kalb K, Hafellner J, Staiger B (1995) Haematomma–Studien II. Lichenicole Pilze auf Arten der Flechtengattung Haematomma. Bibl Lich 59:199–222

    Google Scholar 

  • Kang JC, Kong R, Hyde KD (1998) Studies on the Amphisphaeriales l. Amphisphaeriaceae (sensu stricto) and its phylogenetic relationships inferred from 5.8S rDNAand ITS2 sequences. Fungal Divers 1:147–157

    Google Scholar 

  • Kang HJ, Sigler L, Lee J, Gibas CFC, Yun SH, Lee YW (2010) Xylogone ganodermophthora sp. nov., an ascomycetous pathogen causing yellow rot on cultivated mushroom Ganoderma lucidum in Korea. Mycologia 102:1167–1184

    CAS  PubMed  Google Scholar 

  • Kantvilas G, Coppins BJ (1997) Melaspilea circumserpens Nyl. rediscovered and referred to Glonium, with discussion on the provenance of some of Robert Brown’s lichen specimens. Lichenologist 29:525–531

    Google Scholar 

  • Kar AK, Maity MK (1971) Leaf–inhabiting pyrenomycetes of West Bengal (India). Mycologia 63:1024–1029

    Google Scholar 

  • Karsten PA (1887) Symbolae ad Mycologiam Fennicam. Pars XXI. Meddn Soc Fauna Flora fenn 14:103–110

    Google Scholar 

  • Kashiwadani H, Aptroot A, Moon KH (2009) New pyrenocarpous lichens in Japan, with the resurrection of the genus Trypetheliopsis for Musaespora. Bibl Lichenologica 99:247–258

    Google Scholar 

  • Kendrick B, DiCosmo F (1979) Teleomorph–anamorph connections in ascomycetes. In: Kendrick B (ed) The whole fungus. National Museums of Canada, Ottawa, pp 283–410

    Google Scholar 

  • Khan JA, Hussain ST, Hasan S, McEvoy P, Sarwari A (2000) Disseminated bipolaris infection in an immunocompetent host: an atypical presentation. J Pak Med Assoc 50:68–71

    CAS  PubMed  Google Scholar 

  • Khashnobish A, Shearer CA (1996) Phylogenetic relationships in some Leptosphaeria and Phaeosphaeria species. Mycol Res 100:1355–1363

    Google Scholar 

  • Kirchmair M, Neuhauser S, Buzina W, Huber L (2008) The taxonomic position of Roesleria subterranea. Mycol Res 112:1210–1219

    CAS  PubMed  Google Scholar 

  • Kirk PM, Cannon PF, David JC, Stalpers JA (2001) Ainsworth & Bisby’s dictionary of the fungi, 9th edn. CABI, Wallingford

    Google Scholar 

  • Kirk PM, Cannon PF, Minter DW, Stalpers JA (2008) Ainsworth & Bisby’s dictionary of the fungi, 10th edn. CABI, Wallingford

    Google Scholar 

  • Kirschner R, Araúz V, Herbst F, Hofmann TA, Ix S, Nozon T, Piepenbring M (2010) A new species of Puttemansia (Pleosporales) and new records of further Ascomycota from Panama. Sydowia 62:225–241

    Google Scholar 

  • Kirschstein W (1911) Sphaeriales. Kryptogamen–Flora der Mark Brandenburg 7:164–304

    Google Scholar 

  • Kirschstein W (1924) Beitra¨ge zur Kenntnis der Ascomyceten. Verhandlungen des Botanischen Vereins der Provinz Brandenburg 66:23–29

    Google Scholar 

  • Kishi K (1998) Plant diseases in Japan. Zenkoku Noson Kyoiku Kyokai, Tokyo, p 1128

    Google Scholar 

  • Knudsen K, Lendemer JC (2009) Naetrocymbe herrei (Pleosporales; Ascomycetes), a new lichenized saxicolous species from the coast of central California. Opuscula Philolichenum 6:59–64

    Google Scholar 

  • Kobayashi T, Katsumoto K, Abiko K, Abe Y, Kakishima M (1992) Illustrated genera of plant pathogenic fungi in Japan. Zenkoku Noson Kyoiku Kyokai, Tokyo, p 200

    Google Scholar 

  • Kocourková J, Knudsen K (2009) A new species of Stigmidium (Mycosphaerellaceae, Ascomycetes) from western North America. Czech Mycol 61:73–80

    Google Scholar 

  • Kodsueb R, Dhanasekaran V, Aptroot A, Lumyong S, McKenzie EHC, Hyde KD, Jeewon R (2006a) The family Pleosporaceae: intergeneric relationships and phylogenetic perspectives based on sequence analyses of partial 28S rDNA. Mycologia 98:571–583

    CAS  PubMed  Google Scholar 

  • Kodsueb R, Jeewon R, Vijaykrishna D, Mckenzie EHC, Lumyong P, Lumyong S, Hyde KD (2006b) Systematic revision of Tubeufiaceae based on morphological and molecular data. Fungal Divers 21:105–130

    Google Scholar 

  • Kodsueb R, Lumyong S, Ho WH, Hyde KD, McKenzie EHC, Jeewon R (2007) Morphological and molecular characterization of Aquaticheirospora and phylogenetics of Massarinaceae (Pleosporales). Bot J Linn Soc 155:283–296

    Google Scholar 

  • Kohlmeyer J (1963) Zwei neue Ascomyceten gattungen auf Posidonia rhizomen. Nova Hedwigia 6:5–13

    Google Scholar 

  • Kohlmeyer J (1986) Ascocratera manglicola gen. et sp. nov. and key to the marine Loculoascomycetes on mangroves. Can J Bot 64:3036–3042

    Google Scholar 

  • Kohlmeyer J, Kohlmeyer E (1971) Marine fungi from tropical America and Africa. Mycologia 63:831–861

    CAS  PubMed  Google Scholar 

  • Kohlmeyer J, Kohlmeyer B (1979) Marine fungi: the higher fungi. Academic, New York

    Google Scholar 

  • Kohlmeyer J, Schatz S (1985) Aigialus gen. nov. (Ascomycetes) with two new marine species from mangroves. Trans Br Mycol Soc 85:699–707

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1990) Revision of marine species of Didymosphaeria (Ascomycotina). Mycol Res 94:685–690

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1998a) A new marine Xylomyces on Rhizophora from the Caribbean and Hawaii. Fungal Divers 1:159–164

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1998b) Mycophycias, a new genus for the mycobionts of Apophlaea, Ascophyllum and Pelvetia. Syst Ascomycetum 16:1–7

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B, Eriksson OE (1995a) Fungi on Juncus roemerianus. New marine and terrestrial ascomycetes. Mycol Res 100:393–401

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B, Eriksson OE (1995b) Fungi on Juncus roemerianus 2. New dictyosporus ascomycetes. Bot Mar 38:165–174

    Google Scholar 

  • Kohlmeyer J, Hawksworth DL, Volkmann-Kohlmeyer B (2004) Observations on two marine and maritime “borderline” lichens: Mastodia tessellata and Collemopsidium pelvetiae. Mycol Prog 351–356

  • Körber GW (1865) Ergänzungen zum Systema lichenum Germaniae. Parerga lichenologica. (Breslau) pp 385–501

  • Kruys A, Wedin M (2009) Phylogenetic relationships and an assessment of traditionally used taxonomic characters in the Sporormiaceae (Pleosporales, Dothideomycetes, Ascomycota), utilising multigene phylogenies. Syst Biodivers 7:465–478

    Google Scholar 

  • Kruys A, Eriksson OE, Wedin M (2006) Phylogenetic relationships of coprophilous Pleosporales (Dothideomycetes, Ascomycota), and the classification of some bitunicate taxa of unknown position. Mycol Res 110:527–536

    CAS  PubMed  Google Scholar 

  • Kutorga E, Hawksworth DL (1997) A reassessment of the genera referred to the family Patellariaceae (Ascomycota). Syst Ascomycetum 15:1–110

    Google Scholar 

  • Larget B, Simon DL (1999) Markov chain Monte Carlo algorithms for the Bayesian analysis of phylogenetic trees. Mol Biol Evol 16:750–759

    Google Scholar 

  • Larone DH (1995) Medically important fungi. A guide to identification, 3rd edn. ASM Press, Washington

    Google Scholar 

  • Lawrey JD, Diederich P, Nelsen MP, Sikaroodi M, Gillevet PM, Brand AM, van den Boom P (2011) The obligately lichenicolous genus Lichenoconium represents a novel lineage in the Dothideomycetes. Fungal Biol 115:176–187

    CAS  PubMed  Google Scholar 

  • Lawrey JD, Diederich P, Nelsen MP, Freebury C, Broeck DVD, Sikaroodi M, Ertz D (2012) Phylogenetic placement of lichenicolous Phoma species in the Phaeosphaeriaceae (Pleosporales, Dothideomycetes). Fungal Divers 55:195–213

    Google Scholar 

  • Letrouit-Galinou MA, Parguey-Leduc A, Janex-Favre MC (1994) Ascoma structure and ontogenesis in ascomycete systematics. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. NATO ASI, vol 269. Plenum Press, New York and London, pp 23–36

    Google Scholar 

  • Leuchtmann A (1985a) Kulturversuche mit einigen Arten der Gattung Lophiostoma Ces. & De Not. Sydowia 38:158–170

    Google Scholar 

  • Leuchtmann A (1985b) Über Phaeosphaeria Miyake und andere bitunicate Ascomyceten mit mehrfach querseptierten ascosporen. Sydowia 37:75–194

    Google Scholar 

  • Li YM, Haixia Wu, Cheng H, Hyde KD (2011) Morphological studies in Doithideomycetes: Elsinoё (Elsinoaceae), Butleria and three excluded genera. 115:507–520

  • Li H, Sun G, Zhai X, Batzer J, Mayfield D, Crous P, Groenewald J, Gleason M (2012) Dissoconiaceae associated with sooty blotch and flyspeck on fruits in China and the United States. Persoonia 28:113–125

    PubMed Central  PubMed  Google Scholar 

  • Libert MA (1834) Plantae Cryptogamae, quas in Arduenna collegit. Fasc. 3:no. 272

  • Liew ECY, Aptroot A, Hyde KD (2000) Phylogenetic significance of the pseudoparaphyses in Loculoascomycete taxonomy. Mol Phylogenet Evol 16:392–402

    CAS  PubMed  Google Scholar 

  • Liew ECY, Aptroot A, Hyde KD (2002) An evaluation of the monophyly of Massarina based on ribosomal DNA sequences. Mycologia 94:803–813

    CAS  PubMed  Google Scholar 

  • Lindau G (1896) Hysteriineae. In: Engler & Prantl, Naturliche Pflanzenfamilien. I. Teil, I. Abteilung 1:265–278

  • Lindau G (1897) Pyrenomycetineae, Laboulbeniineae. Engler Prantl Nat Pflanzenfamilien Teil I (Leipzig) 1:321–505

    Google Scholar 

  • Lindemuth R, Wirtz N, Lumbsch HT (2001) Phylogenetic analysis of nuclear and mitochondrial DNA sequences supports the view that loculoascomycetes (Ascomycota) are not monophyletic. Mycol Res 105:1176–1181

    CAS  Google Scholar 

  • Link HF (1816) Observationes in ordines plantarum naturales. Mag Ges Naturf Fr Berl 2. 8:25–45

    Google Scholar 

  • Liu D (2011) Piedraiain molecular detection of human fungal pathogens. CPC press. p 958

  • Liu YJ, Hall DB (2004) Body plan evolution of ascomycetes, as inferred from an RNA polymerase II Phylogeny. Proc Natl Acad Sci 101:4507–4512

    CAS  PubMed Central  PubMed  Google Scholar 

  • Liu JK, Chomnunti P, Cai L, Phookamsak R, Chukeatirote E, Jones EBG, Moslem M, Hyde KD (2010) Phylogeny and morphology of Neodeightonia palmicola sp. nov. from palms. Sydowia 62:261–276

    Google Scholar 

  • Liu JK, Phookamsak R, Jones EBG, Zhang Y, Ko-Ko TW, Hu HL, Boonmee S, Doilom M, Chukeatirote E, Bahkali AH, Wang Y, Hyde KD (2011) Astrosphaeriella is polyphyletic, with species in Fissuroma gen. nov., and Neoastrosphaeriella gen. nov. Fungal Divers 51:135–154

    Google Scholar 

  • Liu JK, Phookamsak R, Doilom M, Wiki S, Mei LY, Ariyawansa HA, Boonmee S, Chomnunti P, Dai DQ, Bhat DJ, Romero AI, Xhuang WY, Monkai J, Jones EBG, Chukeatirote E, KoKo TW, Zhoa YC, Wang Y, Hyde KD (2012a) Towards a natural classification of Botryosphaeriales. Fungal Divers 57:149–210

    Google Scholar 

  • Liu Y, Liu Z, Wongkaew S (2012b) Developing characteristics and relationships of Shiraia bambusicoloa with bamboo. Songklanakarin J Sci Technol 43:17–22

    CAS  Google Scholar 

  • Liu YX, Hyde KD, Ariyawansa HA, Li WJ, Zhou DQ, Yang YL, Chen YM, Liu ZY (2013) Shiraiaceae, new family of Pleosporales (Dothideomycetes, Ascomycota). Phytotaxa 103:51–60

    Google Scholar 

  • LoBuglio KF, Berbee ML, Taylor JW (1996) Phylogenetic origins of the asexual mycorrhizal symbiont Cenococcum geophilum Fr. and other mycorrhizal fungi among the ascomycetes. Mol Phylogenet Evol 6:287–294

    CAS  PubMed  Google Scholar 

  • Lohman ML (1932b) Three new species of Mytilidion in the proposed subgenus Lophiopsis. Mycologia 24:477–484

    Google Scholar 

  • Lohman ML (1933a) Hysteriaceae: Life histories of certain species. Pap Mich Acad Sci Arts Lett 17:229–288

    Google Scholar 

  • Lohman ML (1933b) Septonema toruloideum: a stage of Mytilidion scolecosporum. Mycologia 25:34–43

    Google Scholar 

  • Lohman ML (1934) A cultural and taxonomic study of Hysterium hyalinum. Pap Mich Acad Sci Arts Lett 19:133–140

    Google Scholar 

  • Loquin MV (1974) Réorganisation de la systematique des champignons selon les donneés de revolution heliocyclique. Bulletin Mensuel de la Société Linnéenne de Lyon 43, num. spéc. 43:233–238

  • Lorenzo LE, Messuti MI (2005) Glyphium elatum (Ascomycota) in Patagonia (Argentina). Boletin Soc Argent Bot 40:13–16

    Google Scholar 

  • Luck-Allen ER, Cain RF (1975) Additions to the genus Delitschia. Can J Bot 53:1827–1887

    Google Scholar 

  • Lücking R (2008) Foliicolous lichenized fungi. Flora Neotropica Monogr 103:1–866

    Google Scholar 

  • Lücking R, Sérusiaux E (1996) Musaespora kalbii (lichenized Ascomycetes: Melanommatales), a new foliicolous lichen with a pantropical distribution. Nord J Bot 16:661–667

    Google Scholar 

  • Lücking R, Aptroot A, Thor G (1997) New species or interesting records of foliicolous lichens. II. Flavobathelium epiphyllum (lichenized Ascomycetes: Melanommatales). Lichenologist 29:221–228

    Google Scholar 

  • Lücking R, Sérusiaux E, Maia LC, Pereira CG (1998) A revision of the names of foliicolous lichenized fungi published by Batista and co–workers between 1960 and 1975. Lichenologist 30:121–191

    Google Scholar 

  • Lücking R, Sipman HJM, Umaña L, Chaves JL, Lumbsch HT (2007) Aptrootia (Dothideomycetes: Trypetheliaceae), a new genus of pyrenocarpous lichens for Thelenella terricola. Lichenologist 39:187–193

    Google Scholar 

  • Lücking R, Seavey F, Common RS, Beeching SQ, Breuss O, Buck WR, Crane L, Hodges M, Hodkinson BP, Lay E, Lendemer JC, McMullin RT, Mercado-Díaz JA, Nelsen MP, Rivas Plata E, Safranek W, Sanders WB, Schaefer HP Jr, Seavey J (2011) The lichens of Fakahatchee Strand Preserve State Park, Florida: Proceedings from the 18th Tuckerman Workshop. Bull Florida Museum Nat Hist 49:127–186

    Google Scholar 

  • Lumbsch HT (1999) The ascomata development in Mycoporum elabens (Mycoporaceae, Dothidiales). Plant Biol 1:321–326

    Google Scholar 

  • Lumbsch HT, Huhndorf S (2007) Outline of Ascomycota. Myconet 13:1–99

    Google Scholar 

  • Lumbsch HT, Huhndorf SM (2010) Myconet Volume 14. Part one. Outline of Ascomycota 2009. Part Two. Notes on Ascomycete Systematics. Nos. 4751–5113. Fieldiana Life Earth Sci 1:1–64

    Google Scholar 

  • Lumbsch HT, Schmitt I, Lindemuth R, Miller A, Mangold A, Fernandez F, Huhndorf S (2005) Performance of four ribosomal DNA regions to infer higher–level phylogenetic relationships of inoperculate euascomycetes (Leotiomyceta). Mol Phylogenet Evol 34:512–524

    CAS  PubMed  Google Scholar 

  • Lundqvist N (1964) The genus Trichodelitschia in Sweden. Sven Bot Tidskr 58:267–272

    Google Scholar 

  • Luttrell ES (1951) Taxonomy of Pyrenomycetes. Univ Missouri Stud 24(3):1–120

    Google Scholar 

  • Luttrell ES (1955) The ascostromatic Ascomycetes. Mycologia 47:511–532

    Google Scholar 

  • Luttrell ES (1973) Loculoascomycetes. In: Ainsworth GC, Sparrow FK, Sussman AS (eds) The fungi, an advanced treatise, a taxonomic review with keys: ascomycetes and fungi imperfecti. Academic, London, pp 135–219

    Google Scholar 

  • Lutzoni F, Kauff F, Cox CJ, McLaughlin D, Celio G, Dentinger B, Padamsee M, Hibbett D, James TY, Baloch E, Grube M, Reeb V, Hofstetter V, Schoch CL, Arnold AE, Miadlikowska J, Spatafora J, Johnson D, Hambleton S, Crockett M, Shoemaker R, Sung GH, Lücking R, Lumbsch T, O’Donnell K, Binder M, Diederich P, Ertz D, Gueidan C, Hansen K, Harris RC, Hosaka K, Lim YW, Matheny B, Nishida H, Pfister D, Rogers J, Rossman AY, Schmitt I, Sipman H, Stone J, Sugiyama J, Yahr R, Vilgalys R (2004) Assembling the fungal tree of life: progress, classification, and evolution of subcellular traits. Am J Bot 91:1446–1480

    PubMed  Google Scholar 

  • Ma Y, Zhang R, Sun G, Zhu H, Tang M, Batzer JC, Gleason ML (2010) A new species of Zygophiala associated with the flyspeck complex on apple from China. Mycol Prog 9:151–155

    Google Scholar 

  • Malathrakis NE (1979) A study of an olive tree disease caused by the fungus Phoma incompta Sacc. et Mart. Dissertation, Agricultural College of Athens

  • Malloch D (1970) The genera of cleistothecial Ascomycota. Ph.D. Thesis. University of Toronto

  • Malloch D (1981) The plectomycete centrum. In: Reynolds DR (ed) Ascomycete systematics. The Luttrellian concept. Springer–Verlag, New York, pp 73–91

    Google Scholar 

  • Malloch D, Cain R (1971) Four new genera of cleistothecial ascomycetes with hyaline ascospores. Can J Bot 49:847–854

    Google Scholar 

  • Malloch D, Cain RF (1972) New species and combinations of cleistothecial ascomycetes. Can J Bot 50:61–72

    Google Scholar 

  • Malloch D, Sigler L (1988) The Eremomycetaceae (Ascomycotina). Can J Bot 66:1929–1932

    Google Scholar 

  • Manamgoda DS, Cai L, McKenzie EHC, Crous PW, Madrid H, Chukeatirote E, Shivas RG, Tan YP, Hyde KD (2012) A phylogenetic and taxonomic re–evaluation of the Bipolaris, Cochliobolus, Curvularia Complex. Fungal Divers 56:131–144

    Google Scholar 

  • Mangin L, Patouillard N (1913) Les Atichiales, groupe aberrant d’ascomycètes inférieurs. C R Hebdomadaires Seances Acad Sci Paris 154:1475–1481

    Google Scholar 

  • Martin GW (1941) Outline of the Fungi. Studies in Natural History; Iowa University 18:1–64

  • Massalongo AB (1852) Ricerche sull’autonomia dei licheni crostosi e materiali pella loro naturale ordinazione. Frizerio, Verona

    Google Scholar 

  • Massee G (1895) British fungus flora, a classified textbook of mycology 4:538. George Bell & Sons, London

    Google Scholar 

  • Mathiassen G (1989) Some corticolous and lignicolous Pyrenomycetes s. lat. (Ascomycetes) on Salix in Troms, N Norway. Sommerfeltia 9:1–100

    Google Scholar 

  • McCarthy PM (1995) New saxicolous species of Strigula Fr. (lichenised Ascomycotina: Strigulaceae) from Australia and New Zealand. Muelleria 8:323–329

    Google Scholar 

  • McCarthy PM (1997) New and interesting saxicolous species of Strigula. Lichenologist 29:513–523

    Google Scholar 

  • McCarthy PM (2001) The lichen genus Strigula in Christmas Island, Indian Ocean. Bibl Lichenologica 78:275–287

    Google Scholar 

  • McCarthy PM (2009) Strigulaceae. Flora Aust 57:570–584, 593–601

    Google Scholar 

  • McNeill J, Turland NJ, Monro AM, Lepschi BJ (2011) XVIII International Botanical Congress: preliminary mail vote and report of Congress action on nomenclature proposals. Taxon 60:1507–1520

    Google Scholar 

  • Meeker JA (1975) Revision of the Seuratiaceae I. Morphology of Seuratia. Can J Bot 53:2462–2482

    Google Scholar 

  • Messuti MI, Lorenzo LE (1997) A new species of Hysterium from Patagonia, Argentina. Mycol Res 101:302–304

    Google Scholar 

  • Mibey RK, Hawksworth D (1995) Diporothecaceae, a new family of ascomycetes, and the term ‘hyphopodium’. Syst Ascomycetum 14:25–31

    Google Scholar 

  • Miller JH (1928) Biologic studies in the Sphaeriales 1. Mycologia 20:187–213

    Google Scholar 

  • Miller JH (1938) Studies in the development of two Myriangium species and the systematic position of the order Myriangiales. Mycologia 30:158–181

    Google Scholar 

  • Miller JH (1949) A revision of the classification of the Ascomycetes with special emphasis on the Pyrenomycetes. Mycologia 41:99–127

    Google Scholar 

  • Miller JH, Burton MG (1943) Studies in some Venezuelan ascomycetes collected by Chardon CE and Muller AS. Mycologia 35:83–94

    Google Scholar 

  • Miller MA, Pfeiffer W, Schwartz T (2010) Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In: Proceedings of the Gateway Computing Environments Workshop (GCE). San Diego Supercomput. Center, New Orleans, LA. CA pp 1–8

  • Minnis AM, Kennedy AH, Grenier DB, Rehner SA, Bischoff JF (2011) Asperisporium and Pantospora (Mycosphaerellaceae): epitypifications and phylogenetic placement. Persoonia 27:1–8

  • Minnis AM, Kennedy AH, Grenier DB, Palm ME, Rossman AY (2012) Phylogeny and taxonomic revision of the Planistromellaceae including its coelomycetous anamorphs: contributions towardsa monograph of the genus Kellermania. Persoonia 29:11–28

    CAS  PubMed Central  PubMed  Google Scholar 

  • Minter DW, Peredo HL, Watson A (2007) Acrospermum chilense sp. nov. from Chile and the Acrospermales ord. nov. Bol Soc Argent Bot 42:107–112

    Google Scholar 

  • Miyake I (1909) Studies on the parasitic fungi of rice in Japan. Bot Mag Tokyo 23:85–97

    Google Scholar 

  • Monkai J, Liu JK, Boonmee S, Chomnunti P, Chukeatirote E, Jones EBG, Wang Y, Hyde KD (2013) Planistromellaceae (Botryosphaeriales). Cryptogam Mycol 34:45–77

    Google Scholar 

  • Montagne JPFC (1842) Botanique. Plantes cellulaires. In: de la Sagra R (ed) Histoire Physique Politique et Naturelle de l’Ile de Cuba 2:1–549, France

  • Morakotkarn D, Kawasaki H, Tanaka K, Okane I, Seki T (2008) Taxonomic characterization of Shiraia–like fungi isolated from bamboos in Japan. Mycoscience 49:258–265

    CAS  Google Scholar 

  • Moreau C (1953) Les genres Sordaria et Pleurage. Encyclopédie Mycol 25:1–130

    Google Scholar 

  • Mugambi GK, Huhndorf SM (2009a) Molecular phylogenetics of Pleosporales: Melanommataceae and Lophiostomataceae recircumscribed (Plesporomycetidae, Dothideomycetes, Ascomycota). Stud Mycol 64:103–121

    CAS  PubMed Central  PubMed  Google Scholar 

  • Mugambi GK, Huhndorf SM (2009b) Parallel evolution of hysterothecial ascomata in ascolocularous fungi (Ascomycota, Fungi). Syst Biodivers 7:453–464

    Google Scholar 

  • Muggia L, Gueidan C, Knudsen K, Perlmutter G, Grube M (2012) The lichen connections of black fungi. Mycopathologia

  • Müller E (1950) Die schweizerischen Arten der Gattung Leptosphaeria und ihrer Verwandten. Sydowia 4:185–319

    Google Scholar 

  • Müller E, Sanwal BD (1954) Über die Gattungen Microcyclus Sacc., Coccoidella v. Höhn., Coccodothis Theiss. et Syd. und Coccodothella Theiss. et Syd. Sydowia 8:231–244

    Google Scholar 

  • Müller E, von Arx JA (1950) Einige Aspeckte zur Systematik pseudospharialer Ascomyceten. Ber Schweizerischen Botanischen Ges 60:329–397

    Google Scholar 

  • Müller E, von Arx JA (1962) Die Gattungen der didymosporen Pyrenomyceten. Beitr Kryptogamenflora Schweiz 11(2):1–922

    Google Scholar 

  • Müller E, von Arx JA (1973) Pyrenomycetes: Meliolales, Coronophorales, Sphaeriales. New exotic fungi. Grevillea 17(1888):42–43

    Google Scholar 

  • Munk A (1953) The system of the pyrenomycetes. A contribution to a natural classification of the group Sphaeriales sensu Lindau. Dansk Botanisk Arkiv 15:1–163

    Google Scholar 

  • Munk A (1956) On Metasphaeria coccodes (Karst.) Sacc. (Massarinaceae n. fam.). Friesia 5:303–308

    Google Scholar 

  • Munk A (1957) Danish pyrenomycetes. A preliminary flora. Dansk Botanisk Arkiv 17:1–491

    Google Scholar 

  • Muthumeenakshi S, Goldstein AL, Stewart A, Whipps JM (2001) Molecular studies on intraspecific diversity and phylogenetic position of Coniothyrium minitans. Mycol Res 105:1065–1074

    CAS  Google Scholar 

  • MycoBank (2013) http://www.mycobank.org/BioloMICS.aspx?Link=T&TableKey=14682616000000061&Rec=44996&Fields=All

  • Nagasawa E, Otani Y (1977) Some species of the bambusicolous ascomycetes from Japan I. Rep Tottori Mycol Instit 15:38–42

    Google Scholar 

  • Nakagiri A (1984) Two new species of Lulworthia and evaluation of genera–delimiting characters between Lulworthia and Lindra (Halosphaeriaceae). Trans Mycol Soc Jpn 25:377–388

    Google Scholar 

  • Nannfeldt JA (1932) Studien uber die Morphologie und Systematik der nicht–lichenisierten, inoperkulaten Discomyceten. Nova Acta Regiae Soc Sci Uppsaliensis IV 8:1–368

    Google Scholar 

  • Navarro-Rosinés P, Hafellner J (1996) Lichenostigma elongata spec. nov. (Dothideales), a lichenicolous ascomycete on Lobothallia and Aspicilia species. Mycotaxon 57:211–225

    Google Scholar 

  • Nelsen MP, Lücking R, Grube M, Mbatchou JS, Muggia L, Rivas-Plata E, Lumbsch HT (2009) Unravelling the phylogenetic relationships of lichenised fungi in Dothideomyceta. Stud Mycol 64:135–144

    CAS  PubMed Central  PubMed  Google Scholar 

  • Nelsen MP, Lücking R, Mbatchou JS, Andrew CJ, Spielmann AA, Lumbsch HT (2011a) New insights into relationships of lichen–forming Dothideomycetes. Fungal Divers 51:155–162

    Google Scholar 

  • Nelsen MP, Rivas Plata E, Andrew CJ, Lücking R, Lumbsch HT (2011b) Phylogenetic diversity of trentepohlialean algae associated with lichen–forming fungi. J Phycol 47:282–290

    Google Scholar 

  • Nelsen MP, Lücking R, Aptroot A, Cáceres MES, Lumbsch HT (2013) Attaining the phylogenetic disposition of Aspidotheliacea (Ascomycota), an orphaned family of lichen–forming fungi. In prep

  • Nelson S (2008) Citrus scab. Plant Dis 60:1–6

    Google Scholar 

  • Nelson PE, Wilhelm S (1956) An undescribed fungus causing a root rot of strawberry. Mycologia 48:547–551

    Google Scholar 

  • Nitschke TRJ (1869) Grundlage eines Systems der Pyrenomyceten. Verhandlungen des Naturhistorischen Vereins der Preussischen Rheinlande, Westfalens und des Regierungsbezirks Osnabrück 26:70–77

  • Nylander W (1854) Essai d’une nouvelle classification des Lichens. Mém Soc Imp Sci Nat Cherbourg 2:5–16

    Google Scholar 

  • Nylander JAA (2004) MrModeltest 2.0. Program distributed by the author. Evolutionary Biology Centre, Uppsala University

  • Olivier C, Berbee ML, Shoemaker RA, Loria R (2000) Molecular phylogenetic support from ribosomal DNA sequences for origin of Helminthosporium from Leptosphaeria–like loculoascomycete ancestors. Mycologia 92:736–746

    CAS  Google Scholar 

  • Orange A (2009) Lichenicolous fungi on Ionaspis lacustris. Mycotaxon 81:265–280

    Google Scholar 

  • Orton CR (1924) Studies in the morphology of the Ascomycetes I. The stroma and the compound fructification of the Dothideaceae and other groups. Mycologia 16:49–95

    Google Scholar 

  • Padhye AA, Gutekunst RW, Smith DJ, Punithalingam E (1997) Maxillary sinusitis caused by Pleurophomopsis lignicola. J Clin Microbiol 35(8):2136

    CAS  PubMed Central  PubMed  Google Scholar 

  • Page RDM (1996) TreeView: an application to display phylogenetic trees on personal computers. Comput Appl Biosci 12:357–358

    CAS  PubMed  Google Scholar 

  • Pang KL, Abdel-Wahab MA, Sivichai S, El-Sharouney H, Jones EBG (2002) Jahnulales (Dothideomycetes, Ascomycota): a new order of lignicolous freshwater ascomycetes. Mycol Res 106:1031–1042

    Google Scholar 

  • Pang KL, Jheng JS, Jones EBG (2011) Marine mangrove fungi of Taiwan. National Taiwan Ocean University Press, Keelung, pp 1–131

    Google Scholar 

  • Pang KL, Hyde KD, Alias SA, Suetrong S, Jones EBG (2013) Dyfrolomycetaceae, a new family in the Dothideomycetes, Ascomycota. Cryptogamie Mycologie

  • Peever TL, Barve MP, Stone LJ, Kaiser WJ (2007) Evolutionary relationships among Ascochyta species infecting wild and cultivated hosts in the legume tribes Cicereae and Vicieae. Mycologia 99:59–77

    CAS  PubMed  Google Scholar 

  • Penzig G, Saccardo PA (1898) Diagnoses fungorum novorum in insula Java collectorum. Ser. II. Malpighia 11:491–530

    Google Scholar 

  • Pereira OL, Barreto RW (2003) Anhellia verruco–scopiformans sp. nov. (Myriangiales) associated with scaby brooms of Croton migrans in Brazil. Fungal Divers 12:155–159

    Google Scholar 

  • Pérez CA, Wingfield MJ, Altier NA, Blanchette RA (2009) Mycosphaerellaceae and Teratosphaeriaceae associated with Eucalyptus leaf diseases and stem cankers in Uruguay. For Pathol 39:349–360

    Google Scholar 

  • Pérez-Ortega S, Ríos Ade L, Crespo A, Sancho LG (2010) Symbiotic lifestyle and phylogenetic relationships of the bionts of Mastodia tessellata (ascomycota, incertae sedis). Am J Bot 97:738–752

    PubMed  Google Scholar 

  • Persoon CH (1800) Icones et description Fugorum-minus cognitorum 2: 27–67 Lispsiae

  • Persoon CH (1801) Synopsis Methodica Fungorum, Henrich Dieterich Publ. 706 pages. Gottingae

  • Petrak F (1923a) Mykologische Notizen VI. No. 226. Über die Gattung Glonium Müh. Ann Mycol 21:225–227

    Google Scholar 

  • Petrak F (1923b) Mykologische Notizen VI. No. 284. Psiloglonium finkii nov. sp. Ann Mycol 21:308–309

    Google Scholar 

  • Petrak F (1934) Mykologische Notizen. XII. Nos. 751–850. Ann Mycol 32:317–447

    Google Scholar 

  • Petrak F (1947) Über die Leptopeltineen. Sydowia 1:232–247

    Google Scholar 

  • Petrak F (1952) Ergebnisse einer Revision der Grundtypen verschiedener Gattungen der Askomyzeten und Fungi Imperfecti. III. Sydowia 6:336–343

    Google Scholar 

  • Petrak F (1953) Die Gattung Blasdalea Sacc. et Syd. Sydowia 7:343

    Google Scholar 

  • Petrak F (1962) Uber die Gattung Saccardoella Speg. Sydowia 15:233–236

    Google Scholar 

  • Petrak F, Ciferri R (1932) Fungi Dominicani. II. Ann Mycol 30:149–353

    Google Scholar 

  • Petrak F, Sydow H (1929) Kritisch–systematische Original untersuchungen über Pyrenomyzeten, Sphaeropsideen und Melanconieen: IV. Ann Mycol 27:87–115

    Google Scholar 

  • Petrini O, Samuels GL, Müller E (1979) Holmiella sabina (de Not.) comb. nov. (syn. Eutryblidiella sabina) and its Cornicularia–like anamorph, an endophyte on Juniperus species. BerSchweizerischen Botanischen Ges 89:80–90

    Google Scholar 

  • Phillips AJL, Alves A, Pennycook SR, Johnston PR, Ramaley A, Akulov A, Crous PW (2008) Resolving the phylogenetic and taxonomic status of dark–spored teleomorph genera in the Botryosphaeriaceae. Persoonia 21:29–55

    CAS  PubMed Central  PubMed  Google Scholar 

  • Phongpaicht S, Tanaka K, Hairayama K, Jones EBG (2009) Molecular systematics of the marine Dothideomycetes. Stud Mycol 64:155–173

    Google Scholar 

  • Pinokiyo A, Singh KP (2006) New species and new record of foliicolous lichenized fungi from Sikkim (India). Mycotaxon 97:57–60

    Google Scholar 

  • Pinruan U, Jones EBG, Hyde KD (2002) Aquatic fungi from peat swamp palms: Jahnula appendiculata sp. nov. Sydowia 54:242–247

    Google Scholar 

  • Pirozynski KA (1972) Microfungi of Tanzania. I. Miscellaneous fungi on oil palm. II. New hyphomycetes. Mycol Pap 12:1–64

    Google Scholar 

  • Pirozynski KA (1974) Meliolina mollis and two hypersites in India. Kavaka 2:33–41

    Google Scholar 

  • Pirozynski KA, Shoemaker R (1970) Some Asterinaceae and Meliolaceae on conifers in Canada. Can J Bot 48:1321–1328

    Google Scholar 

  • Plemenitaš A, Vaupotič T, Lenassi M, Kogej T, Gunde-Cimerman N (2008) Adaptation of extremely halotolerant black yeast Hortaeawerneckii to increased osmolarity: a molecular perspective at a glance. Stud Mycol 61:67–75

    PubMed Central  PubMed  Google Scholar 

  • Poelt J (1969) Bastimmungsschlüssel europäischer Flechten. Cramer, Lehre

    Google Scholar 

  • Poelt J (1974) Classification. In: Ahmadjian V, Hale ME (eds) The lichens. New York Academic Press, p 599–632

  • Promputtha I, Miller AN (2010) Three new species of Acanthostigma (Tubeufiaceae, Pleosporales) from the Great Smoky Mountains National Park. Mycologia 102(3):574–587

    PubMed  Google Scholar 

  • Punithalingam E (1969) Studies on Sphaeropsidales in culture. Mycol Pap 119:1–24

    Google Scholar 

  • Quaedvlieg W, Kema GHJ, Groenewald JZ, Verkley GJM, Seifbarghi S, Razavi M, Mirzadi Gohari A, Mehrabi R, Crous PW (2011) Zymoseptoria gen. nov.: a new genus to accommodate Septoria-like speciesoccurring on graminicolous hosts. Persoonia 26:57–69

    CAS  PubMed Central  PubMed  Google Scholar 

  • Quaedvlieg W, Groenewald JZ, De Jesús Yáñez–Morales M, Crous PW (2012) DNA barcoding of Mycosphaerella species of quarantine importance to Europe. Persoonia 29:101–115

    CAS  PubMed Central  PubMed  Google Scholar 

  • Quaedvlieg W, Verkley GJM, Shin H-D, Barretto RW, Alfenas AC, Swart WJ, Groenewald JZ, Crous PW (2013) Sizing up Septoria. Stud Mycol 75:307–390

    Google Scholar 

  • Rabenhorst L (1863) Fungi Europaei Exsiccati. Editio novo. Century VI (nos 501–600). Dresden

  • Raciborski M (1900) Parasitische. Algen und Pilze Java’s. I. Theil. Staatsdruckerei. Batavia, p 39

  • Raja HA, Shearer CA (2006) Jahnula species from North and Central America, including three new species. Mycologia 98:312–332

    Google Scholar 

  • Raja HA, Shearer CA (2008) Freshwater ascomycetes: new and noteworthy species from aquatic habitats in Florida. Mycologia 100:467–489

    PubMed  Google Scholar 

  • Raja HA, Schoch CL, Hustad V, Shearer C, Miller A (2011) Testing the phylogenetic utility of MCM7 in the Ascomycota. MycoKeys 1:63–94

    Google Scholar 

  • Raja HA, Miller AN, Shearer CA (2012) Freshwater ascomycetes: Natipusillaceae, a new family of tropical fungi, including Natipusilla bellaspora sp. nov. from the Peruvian Amazon. Mycologia 104:569–573

    PubMed  Google Scholar 

  • Raja HA, Oberlies NH, Tamam-El Elimat, Miller AN, Zelski SE, Shearer CA (2013a) Lindgomyces angustiascus, (Lindgomycetaceae, Pleosporales, Dothideomycetes), a new lignicolous species from freshwater habitats in the USA. Mycoscience, in press

  • Raja HA, Tanaka K, Hirayama K, Hashimoto A, Oberlies NH, Figueroa M, Miller AN, Zelski SE, Shearer CA (2013b) Freshwater ascomycetes: Minutisphaera (Dothideomycetes) revisited, including one new species from Japan. Mycologia in press

  • Rajeshkumar KC, Sharma R (2013) Tamhinispora a new genus belongs to family Tubeufiaceae from the Western Ghats, India based on morphology and phylogenetic analysis. Mycosphere 4:165–174

    Google Scholar 

  • Ramaley AW (1991) Fungi of Yucca baccata. 1. Piptarthron pluriloculare and its teleomorph, Planistroma yuccigena. Mycotaxon 42:63–75

    Google Scholar 

  • Ramaley AW (1992) Fungi from Yucca baccata. 2. Planistroma obtusilunatum sp. nov. and its anamorph Piptarthron uniloculare sp. nov. Mycotaxon 45:449–460

    Google Scholar 

  • Ramaley AW (1993) New fungi from Yucca: Planistromella yuccifoliorum, gen. et sp. nov. and its anamorph Kellermania yuccifoliorum, sp. nov. and Planistromella uniseptata sp. nov. the teleomorph of Kellermania yuccigena. Mycotaxon 47:259–274

    Google Scholar 

  • Ramaley AW (1995) New species of Kellermania, Piptarthron, Planistroma, Planistromella from members of the Agavaceae. Mycotaxon 50:255–268

    Google Scholar 

  • Ramaley AW (1998) New teleomorphs of the anamorphic genus Kellermania. Mycotaxon 66:509–514

    Google Scholar 

  • Ramaley AW (1999) Three species of Microthyrium from Nolina. Mycotaxon 70:7–16

    Google Scholar 

  • Ramaley AW (2005) The connection of Dothidotthia aspera (Botryosphaeriaceae) to a hyphomycetous anamorphic fungus, Thyrostroma negundinis. Mycotaxon 94:127–132

    Google Scholar 

  • Ramaley AW, Barr ME (1995) New dictyosporous species from leaves of Agavaceae. Mycotaxon 54:75–90

    Google Scholar 

  • Rannala B, Yang Z (1996) Probability distribution of molecular evolutionary trees: a new method of phylogenetic inference. J Mol Evol 43:304–311

    Google Scholar 

  • Ranghoo VM, Hyde KD (2000) Ascominuta lignicola, a new loculoascomycete from submerged wood in Hong Kong. Mycoscience 42:1–5

    Google Scholar 

  • Read SJ, Moss ST, Jones EBG (1997) Ultrastructure of asci, ascospores and appendages of Massarina ramunculicola (Loculoascomycetes, Ascomycota). Bot Mar 40:465–471

    Google Scholar 

  • Reddy PV, Patel R, White JF Jr (1998) Phylogenetic and developmental evidence supporting reclassification of cruciferous pathogens Phoma lingam and Phoma wasabiae in Plenodomus. Can J Bot 76:1916–1922

    Google Scholar 

  • Reed M (1902) Two new ascomycetous fungi parasitic on marine algae. Univ Calif Publ Bot 1:141–164

    Google Scholar 

  • Rehm H (1896) Ascomyceten: hysteriaceen und discomyceten. In: Rabenhorst’s L (ed) Kryptogamen–Flora von Deutschland, Oesterreich und der Schweiz, 2nd edn. Eduard Kummer, Leipzig, pp 1–56

    Google Scholar 

  • Rehm H (1900) Beiträge zur Pilzflora von Südamerika VIII. Discomycetes (Nachtrag). IX. Hypocreaceae. X. Dothideaceae. Hedwigia 39:209–234

    Google Scholar 

  • Reid J, Pirozynski KA (1966) Studies on the Patellariaceae. I. Eutrblidiella Sabina (De Not.) Hӧhn. Can J Bot 44:655–662

  • Reid J, Pirozynski KA (1966) Notes on some interesting North American Fungi. Can J Bot 44:649–652

    Google Scholar 

  • Renobales G, Aguirre B (1990) The nomenclature and systematic position of the genus Encephalographa. Syst Ascomycetum 8:87–92

    Google Scholar 

  • Reynolds DR (1971) The sooty mold ascomycetes genus Limacinula. Mycologia 63:1173–1209

    Google Scholar 

  • Reynolds DR (1982) Foliicolous ascomycetes: 4. The capnodiaceous genus Trichomerium Spegazzini emend. Mycotaxon 14:189–220

    Google Scholar 

  • Reynolds DR (1986) Folliicolous ascomycetes 7. Phylogenetic Systematics of the Capnodiaceae. Mycotaxon 27:377–403

    Google Scholar 

  • Reynolds DR, Gilbert GS (2005) Epifoliar fungi from Queensland, Australia. Aust Syst Bot 18:265–289

    Google Scholar 

  • Reynolds DR, Gilbert GS (2006) Epifoliar fungi from Panama. Cryptogam Mycol 27:249–270

    Google Scholar 

  • Riddle LW (1917) Pyrenothrix nigra gen. et spec. nov. Bot Gaz 64:513–515

    Google Scholar 

  • Riddle LW (1920) Observations on the genus Acrospermum. Mycologia 12:175–181

    Google Scholar 

  • Riddle LW (1923) The lichens of the Isle of Pines. Mycologia 15:68–88

    Google Scholar 

  • Ridley GS, Ramsfield TD (2006) Elsinoё takoropuku sp. nov. infects twigs of Pittosporum tenuifolium in New Zealand. Mycologia 97:1362–1364

    Google Scholar 

  • Riedl H (1961) Die Arten der Gattung Mycoporellum Mull. Arg. sensu A. Zahlbruckner. Catal., nebst Bemerkungen zum System dothidealer Flechten. Sydowia 15:257–287

    Google Scholar 

  • Rivas Plata E, Lumbsch HT, Lücking R (2012) A new classification for the lichen family Graphidaceae s.lat. (Ascomycota: Lecanoromycetes: Ostropales). Fungal Divers 52:107–121

    Google Scholar 

  • Rodrigues KF, Samuels GJ (1994) Letendraeopsis palmarum, a new genus and species of Loculoascomycetes. Mycologia 86:254–258

    Google Scholar 

  • Rogers DP (1953) Disposition of nomina generica conservanda for fungi. Taxon 2:29–32

    Google Scholar 

  • Romero AI, Samuels GJ (1991) Studies on Xylophilous fungi from Argentina. VI. Ascomycotina on Eucalyptus viminalis (Myrtaceae). Sydowia 43:228–248

    Google Scholar 

  • Rossman AY (1987) The Tubeufiaceae and similar Loculoascomycetes. Mycol Pap 157:1–71

    Google Scholar 

  • Rossman AY, Mouchacca J, Samuels GJ (1994) Phillipsiella crescentiae comb. nov. and a redescription of P. atra, type of the genus Phillipsiella. Sydowia 46:66–74

    Google Scholar 

  • Rossman AY, Samuels GJ, Rogerson CT, Lowen R (1999) Checklist of genera of Bionectriaceae, Hypocreaceae, Nectriaceae, with an account of excluded genera and species. Stud Mycol 42:1–215

    Google Scholar 

  • Routien JB (1958) A new species of Teichosporella. Mycologia 50:117–120

    Google Scholar 

  • Roux C (2009) Naetrocymbe saxicola, likeno kun Trentepohlia. Bull Soc Linnéenne Provence 60:127–142

    Google Scholar 

  • Roux C, Triebel D (1994) Révision des espèces de Stigmidium et de Sphaerellothecium (champignons lichénicoles non lichénisés, Ascomycetes) correspondant à Pharcidia epicymatia sensu Keissler ou à Stigmidium schaereri auct. Bull Soc Linéenne de Provence 45:451–542

    Google Scholar 

  • Ruibal C, Gueidan C, Selbmann L, Gorbushina AA, Crous PW, Groenewald JZ, Muggia L, Grube M, Isola D, Schoch CL, Staley JT, Lutzoni F, de Hoog GS (2009) Phylogeny of rock–inhabiting fungi related to Dothideomycetes. Stud Mycol 64:123–133

    CAS  PubMed Central  PubMed  Google Scholar 

  • Ryan BD, Bungartz F, Hagedorn G, Rambold G (eds) (2005 onwards) LIAS glossary. A Wiki–based online dictionary for ascomycete terminology used by LIAS, the global information system for lichenized and non–lichenized ascomycetes. http://glossary.lias.net/

  • Saccardo PA (1875) Grevillea 4(29):21

    Google Scholar 

  • Saccardo PA (1877) Fungi venetino vive criticive Mycologiae Venetae addendi. Michelia 1–72

  • Saccardo PA (1878) Fungi Veneti novi vel critici vel mycologiae Venetae addendi. Ser. IX. Michelia 1(4):407

    Google Scholar 

  • Saccardo PA (1880) Fungi Gallici ser. II. Michelia 2:39–135

    Google Scholar 

  • Saccardo PA (1882) Sylloge Fungorum 1, Padova, p 766

  • Saccardo PA (1883) Sylloge Fungorum. 2, Italy, Patavii, pp 1–815

  • Saccardo PA (1891) Sylloge Fungorum 9, Italy, Pavia, p 1141

  • Saccardo PA, Paoletti G (1888) Mycetes Malacenses. Funghi della penisola di Malacca raccolti nel 1885 dell’ Ab. Benedetto Scortechini 6:387–428

    Google Scholar 

  • Saccardo PA, Saccardo D (1905) Supplementum universale. Pars VI. Hymenomycetae–Laboulbeniomycetae. Syll Fung 17:860

    Google Scholar 

  • Saccardo PA, Sydow P (1899) Sylloge Fungorum 14(1):1–724

    Google Scholar 

  • Saccardo PA, Sydow P (1902) Supplementum Universale, Pars V. Syll Fung 16:1–1291

    Google Scholar 

  • Saccardo PA, Trotter A (1913) Supplementum Universale Pars IX. Sylloge Fungorum 22:1–1612

    Google Scholar 

  • Saenz GS, Taylor JW (1999) Phylogenetic relationships of Meliola and Meliolina inferred from nuclear small subunit rRNA sequences. Mycol Res 103:1049–1056

    Google Scholar 

  • Samson RA, Mouchacca J (1975) Two new soil–borne cleistothecial ascomycetes. Can J Bot 53:1634–1639

    Google Scholar 

  • Samuels GJ, Romero AI (1991) Ascoporia (Fungi, Loculoascomycetes), a new genus from Para. Bol Museu Paraense Emilio Goeldi Ser Bot 7:263–268

    Google Scholar 

  • Samuels GJ, Muller E (1979) Life history of Brazilian ascomycetes 6. Sydowia 31:180–193

    Google Scholar 

  • Sanchez RM, Bianchinotti MV (2010) New records in the Tubeufiaceae from Andean Patagonian forests of Argentina. Mycotaxon 111:131–141

    Google Scholar 

  • Sánchez RM, Miller AN, Bianchinotti MV (2012) A new species of Acanthostigma (Tubeufiaceae, Dothideomycetes) from the southern hemisphere. Mycologia 104:223–231

    PubMed  Google Scholar 

  • Sanderson NA, Coppins BJ (2009a) Mycoporum. In: Smith CW, Aptroot A, Coppins BJ, Fletcher A, Gilbert OL, James PW, Wolseley PA (eds) The lichens of Great Britain and Ireland. British Lichen Society, London, pp 620–622

    Google Scholar 

  • Sanderson NA, Coppins BJ (2009b) Tomasellia. In: Smith CW, Aptroot A, Coppins BJ, Fletcher A, Gilbert OL, James PW, Wolseley PA (eds) The lichens of Great Britain and Ireland. British Lichen Society, London, pp 894–895

    Google Scholar 

  • Sanderson NA, Hawksworth DL, Aptroot A (2009) Melaspilea Nyl. In: The lichens of Great Britain and Ireland. British Lichen Society pp 576–579

  • Sankaran KV, Sutton BC (1991) Compsosporiella deightonii gen. et sp. nov. (Coelomycetes) from Sierra Leone. Mycol Res 11:1289–1293

    Google Scholar 

  • Santesson R (1952) Foliicolous lichens I. A revision of the taxonomy of the obligately foliicolous, lichenized fungi. Symbolae Botanicae Upsalienses 12:1–590

    Google Scholar 

  • Sawada K (1959) Descriptive catalogue of Taiwan (Formosan) fungi. Part XI. Spec Publ Coll Agric National Taiwan Univ 8:1–268

    Google Scholar 

  • Schatz S (1984) The life history, developmental morphology, and taxonomy of Lautitia danica gen. nov. comb. nov. Can J Bot 62:28–32

    Google Scholar 

  • Scheinpflug H (1958) Untersuchungen über die Gattung Didymosphaeria Fuck. und einige verwandte Gattungen. Ber Schweizerischen Botanischen Ges 68:325–385

    Google Scholar 

  • Scheuer C (1991) Massarina tetraploa sp. nov. the teleomorph of Tetraploa aristata. Mycol Res 95:126–128

    Google Scholar 

  • Scheuer C, Nograsek A (1993) Trematosphaeria pachycarpa and Herbampulla crassirostris gen. et spec. nov. (Ascomycetes). Mycotaxon 47:415–424

    Google Scholar 

  • Schilling F (1927) Entwicklungsgeschichtliche und systematische Untersuchungen epiphyller Flechten. Hedwigia 67:269–300

    Google Scholar 

  • Schmitt I, Mueller G, Lumbsch HT (2005) Ascoma morphology is homoplaseous and phylogenetically misleading in some pyrenocarpous lichens. Mycologia 97:362–374

    CAS  PubMed  Google Scholar 

  • Schoch CL, Shoemaker RA, Seifert KA, Hambleton S, Spatafora JW, Crous PW (2006) A multigene phylogeny of the Dothideomycetes using four nuclear loci. Mycologia 98:1041–1052

    CAS  PubMed  Google Scholar 

  • Schoch CL, Crous PW, Groenewald JZ, Boehm EWA, Burgess TI, de Gruyter J, de Hoog GS, Dixon LJ, Grube M, Gueidan C, Harada Y, Hatakeyama S, Hirayama K, Hosoya T, Huhndorf SM, Hyde KD, Jones EBG, Kohlmeyer J, Kruys Å, Li YM, Lücking R, Lumbsch HT, Marvanová L, Mbatchou JS, McVay AH, Miller AN, Mugambi GK, Muggia L, Nelsen MP, Nelson P, Owensby CA, Phillips AJL, Phongpaichit S, Pointing SB, Pujade-Renaud V, Raja HA, Rivas Plata E, Robbertse B, Ruibal C, Sakayaroj J, Sano T, Selbmann L, Shearer CA, Shirouzu T, Slippers B, Suetrong S, Tanaka K, Volkmann-Kohlmeyer B, Wingfield MJ, Wood AR, Woudenberg JHC, Yonezawa H, Zhang Y, Spatafora JW (2009a) A class–wide phylogenetic assessment of Dothideomycetes. Stud Mycol 64:1–15

    CAS  PubMed Central  PubMed  Google Scholar 

  • Schoch CL, Sung GH, López-Giráldez F, Townsend JP, Miadlikowska J, Hofstetter V, Robbertse B, Matheny PB, Kauff F, Wang Z, Gueidan C, Andrie RM, Trippe K, Ciufetti LM, Wynns A, Fraker E, Hodkinson BP, Bonito G, Groenewald JZ, Arzanlou M, de Hoog GS, Crous PW, Hewitt D, Pfister DH, Peterson K, Gryzenhout M, Wingfield MJ, Aptroot A, Suh SO, Blackwell M, Hillis DM, Griffith GW, Castlebury LA, Rossman AY, Lumbsch HT, Lücking R, Büdel B, Rauhut A, Diederich P, Ertz D, Geiser DM, Hosaka K, Inderbitzin P, Kohlmeyer J, Volkmann-Kohlmeyer B, Mostert L, O’Donnell K, Sipman H, Rogers JD, Shoemaker RA, Sugiyama J, Summerbell RC, Untereiner W, Johnston PR, Stenroos S, Zuccaro A, Dyer PS, Crittenden PD, Cole MS, Hansen K, Trappe JM, Yahr R, Lutzoni F, Spatafora JW, Schoch CL et al (2009b) The Ascomycota tree of life: a phylum–wide phylogeny clarifies the origin and evolution of fundamental reproductive and ecological traits. Syst Biol 58:224–239

    CAS  PubMed  Google Scholar 

  • Schubert K, Ritschel A, Braun U (2003) A monograph of Fusicladium s. lat. (hyphomycetes). Schlechtendalia 9:1–132

    Google Scholar 

  • Seaver FJ, Chardón CE (1926) Botany of Porto Rico and the Virgin Islands. Mycology. Scientific Survey of Porto Rico and the Virgin Islands 1:40–41

    Google Scholar 

  • Seifert K, Morgan-Jones G, Gams W, Kendrick B (2011) The genera of hyphomycetes. CBS–KNAW Fungal Biodiversity Centre, Utrecht

    Google Scholar 

  • Selbmann L, de Hoog GS, Gerrits van den Ende AHG, Ruibal C, De Leo F, Zucconi L, Isola D, Ruisi S, Onofri S (2005) Drought meets acid: three new genera in a Dothidealean clade of extremotolerant fungi. Stud Mycol 61:1–20

    Google Scholar 

  • Sérusiaux E, Aptroot A (1998) A further new species of Monoblastia (lichenized Ascomycetes: Monoblastiaceae) from Papua New Guinea. Nova Hedwigia 67:259–265

    Google Scholar 

  • Sérusiaux E, Lücking R (2003) The lichen genus Caprettia Bat. & H. Maia (Monoblastiaceae). Bibl Lichenologica 86:161–176

    Google Scholar 

  • Shearer CA (1993) A new species of Kirschsteiniothelia (Pleosporales) with an unusual fissitunicate ascus. Mycologia 85:963–969

    Google Scholar 

  • Shearer CA, Crane JL (1980) Taxonomy of two cleistothecial ascomycetes with papilionaceous ascospores. Trans Br Mycol Soc 75:193–200

    Google Scholar 

  • Shearer CA, Hyde KD (1997) Massarina ingoldiana, a new ascomycete from freshwater habitats. Mycologia 89:114–119

    Google Scholar 

  • Shearer CA, Crane JL, Redy KRC (1990) Studies in Leptosphearia. Lectotypification of Sphaeria dolioum. Mycologia 82:496–500

    Google Scholar 

  • Shearer CA, Raja HA, Miller AN, Nelson P, Tanaka K, Hirayama K, Marvanova L, Hyde KD, Zhang Y (2009) The molecular phylogeny of freshwater Dothideomycetes. Stud Mycol 64:145–153

    CAS  PubMed Central  PubMed  Google Scholar 

  • Shenoy BD, Jeewon R, Wu WP, Bhat DJ, Hyde KD (2006) Ribosomal an dRPB2 DNA sequence analyses suggest that Sporidesmium and morphologicaly similar genera are polyphyletic. Mycol Res 110:916–928

    CAS  PubMed  Google Scholar 

  • Sherwood MA (1977) The ostropalean fungi. Mycotaxon 5:1–277

    Google Scholar 

  • Sherwood MA (1979) Helochora, a new genus of Polystigmataceae. Mycologia 71:648–651

    Google Scholar 

  • Sherwood-Pike M, Boise J (1986) Studies in lignicolous ascomycetes: Xylopezia and mycowinteria. Brittonia 38:35–44

    Google Scholar 

  • Shoemaker RA (1963) Generic correlations and concepts: Griphosphaerioma and Labridella. Can J Bot 41:1419–1423

    Google Scholar 

  • Shoemaker RA, Babcock CE (1989) Phaeosphaeria. Can J Bot 67:1500–1599

    Google Scholar 

  • Shoemaker RA, Babcock CE (1992) Applanodictyosporous Pleosporales: Clathrospora, Comoclathris, Graphyllium, Macrospora, and Platysporoides. Can J Bot 70:1618

    Google Scholar 

  • Shoemaker RA, Egger KN (1982) Piedraia hortae. Fungi Canadenses 211:1–2

    Google Scholar 

  • Shoemaker RA, Holm L, Eriksson OE (2003) Proposal to conserve the name Dothidea with a conserved type (Fungi: Dothideomycetes). Taxon 52:623–625

    Google Scholar 

  • Sierra DL (2006) Contribución al estudio de los Ascomicetes bitunicados de Botanica Barcinonensia 50:5–434

  • Sigler L, Lumley TC, Currah RS (2000) New species and records of saprophytic ascomycetes (Myxotrichaceae) from decaying logs in the boreal forest. Mycoscience 41:495–502

    Google Scholar 

  • Silva-Hanlin DMW, Hanlin RT (1999) Small subunit ribosomal RNA gene phylogeny of several Loculoascomycetes and its taxonomic implications. Mycol Res 103:153–160

    Google Scholar 

  • Simon UK, Groenewald JZ, Crous PW (2009) Cymadothea trifolii, an obligate biotrophic leaf parasite of Trifolium, belongs to Mycosphaerellaceae as shown by nuclear ribosomal DNA analyses. Persoonia 22:49–55

    CAS  PubMed Central  PubMed  Google Scholar 

  • Sivanesan A (1977) The taxonomy and pathology of Venturia species. Lubrecht & Cramer Ltd, Vaduz, 138

    Google Scholar 

  • Sivanesan A (1981) Balladynopsis, Balladynocallia and Alina. Mycol Pap 146:1–38

    Google Scholar 

  • Sivanesan A (1984) The bitunicate ascomycetes and their anamorphs. J. Cramer, Vaduz, p 701

    Google Scholar 

  • Sivanesan A (1996) Corynesporasca caryotae gen. et sp. nov. with a Corynespora anamorph, and the family Corynesporascaceae. Mycol Res 100:783–788

    Google Scholar 

  • Sivanesan A, Hsieh WH (1989) Kentingia and Setocampanula, two new ascomycete genera. Mycol Res 93(1):83–90

    Google Scholar 

  • Slippers B, Crous PW, Denman S, Coutinho TA, Wingfield BD, Wingfield MJ (2004) Combined multiple gene genealogies and phenotypic characters differentiate several species previously identified as Botryosphaeria dothidea. Mycologia 96:83–101

    CAS  PubMed  Google Scholar 

  • Smith CW, Aptroot A, Coppins BJ, Fletcher A, Gilbert OL, James PW, Wolseley PA (eds) (2009) The lichens of Great Britain and Ireland. The British Lichen Society, London, p 1046

    Google Scholar 

  • Spatafora JW, Owensby CA, Douhan G, Boehm EWA, Schoch C (2011) Phylogenetic placement of Cenococcum in Gloniaceae (Dothideomycetes). Mycologia 104:758–765

    Google Scholar 

  • Speer EO (1986) A propos de champignons du Brésil III. Mytilidion resinae sp. nov. (Hysteriales) et sa forme conidienne, Camaroglobulus resinae gen. et spec. nov. (Sphaeropsidales). Bull Trimest Soc Mycol Fr 102:97–100

    Google Scholar 

  • Spegazzini C (1879) Nova addenda ad mycologiam venetam. Michelia 1:453–487

    Google Scholar 

  • Spegazzini (1880) Pleomassaria. Anales de la Sociedad Científica Argentina. 9: (in tabula ad p 192)

  • Spegazzini C (1889a) Fungi Puiggariani. Pugillus 1. Bol Acad Nac Cienc Córdoba 11(4):381–622

    Google Scholar 

  • Spegazzini C (1889b) Fungi nonnulli. Paraguariae Fuegiae–Rev Mycol Toulouse (Toulouse) 11(42):93–95

    Google Scholar 

  • Spegazzini C (1909) Mycetes Argentinenses. Series IV. Anales del Museo Nacional de Historia Natural Buenos Aires 19:257–458

  • Spooner BM, Kirk PM (1990) Observations on some genera of Trichothyriaceae. Mycol Res 94:223–230

    Google Scholar 

  • Stamatakis A (2006) RAxML-VI-HPC: Maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22:2688–2690

    Google Scholar 

  • Stamatakis A, Hoover P, Rougemont J (2008) A rapid bootstrap algorithm for the RAxML Web Servers. Syst Biol 57:758–771

    PubMed  Google Scholar 

  • Starbäck K (1899) The Myriangiales Bihang till Kongliga Svenska Vetenskaps Academien Handlingar 25:3–37

  • Stenroos S, Laukka T, Huhtinen S, Döbbeler P, Myllys L, Syrjänen K, Hyvönen J (2010) Multiple origins of symbioses between ascomycetes and bryophytes suggested by a five–gene phylogeny. Cladistics 26:281–300

    Google Scholar 

  • Stevens FL (1917) Porto Rican fungi, old and new. Trans Illinois State Acad Sci 10:162–218

    Google Scholar 

  • Stevens FL (1925) Hawaiian fungi. Bull Bernice P Bishop Museum Honolulu 19:1–189

    Google Scholar 

  • Stizenberger E (1862) Beitrag zur Flechtensystematik. Ber über die Thätigkeit Sankt Gallischen Natuwiss Ges 124–182

  • Stone RE (1912) The life history of Ascochyta on some leguminous plants. Ann Mycol 10:564–592

    Google Scholar 

  • Su D, Ru-jun Z, Xue-rui Y, Shu-yi Y, Jun-Fan F (2012) Infection and establishment of Ascochyta anemones in leaves of windflower. Afr J Microbiol Res 6:4983–4988

    Google Scholar 

  • Suetrong S, Jones EBG (2006) Marine discomycetes: a review. Indian J Mar Sci 35:291–296

    Google Scholar 

  • Suetrong S, Schoch CL, Spatafora JW, Kohlmeyer J, Volkmann-Kohlmeyer B, Sakayaroj J, Phongpaicht S, Tanaka K, Hairayama K, Jones EBG (2009) Molecular systematics of the marine Dothideomycetes. Stud Mycol 64:155–173

    CAS  PubMed Central  PubMed  Google Scholar 

  • Suetrong S, Sakayaroj J, Phongpaichit S, Jones EBG (2010) Morphological and molecular characteristics of a poorly known marine ascomcycete, Manglicola guatamalensis (Jahnulales: Pezizomycotina; Dothideomycetes, Incertae sedis): new lineage of marine ascomycetes. Mycologia 102:83–92

    PubMed  Google Scholar 

  • Suetrong S, Boonyue N, Pang KL, Ueapattanakit J, Klaysuban A, Sri-Inddrasutdhi V, Sivichai S, Jones EBG (2011a) A taxonomic revision and phylogenetic reconstruction of the Jahnulales (Dothideomycetes), and the new family Manglicolaceae. Fungal Divers 51:163–188

    Google Scholar 

  • Suetrong S, Hyde KD, Ahang Y, Bahkali AB, Jones EBG (2011b) Trematosphaeriaceae fam. nov. (Dothideomycetes, Ascomycota). Cryptogam Mycol 32:343–358

    Google Scholar 

  • Suh SO, Blackwell M (1999) Molecular phylogeny of the cleistothecial fungi placed in Cephalothecaceae and Pseudeurotiaceae. Mycologia 91:836–845

    CAS  Google Scholar 

  • Sutton BC (1970) Glyphium leptothecium (Earle) comb. nov. G. schizosporum (Maire) Zogg, and their imperfect states. Trans Br Mycol Soc 54:255–264

    Google Scholar 

  • Sutton BC (1980) The Coelomycetes. Fungi Imperfecti with Pycnidia, Acervuli and Stromata. Commonwealth Mycological Institute pp 1–696

  • Sutton BC, Alcorn JL (1983) Sarcinulella banksiae gen. et sp. nov. a coelomycete with a unique method of conidial dispersal. Mycotaxon 16:557–564

    Google Scholar 

  • Sutton BC, Pollok FG (1973) Gleosporium cercocarpi and Sphaceloma cercocarpi. Mycologia 65:1125–1134

    Google Scholar 

  • Swart HJ (1971) Australian leaf–inhabiting fungi I. Two species of Vizella. Trans Br Mycol Soc 57:455

    Google Scholar 

  • Swart HJ (1987) Australian leaf–inhabiting fungi. XXV. Dothidellainaequalis and Montagnellaeucalypti. Trans Br Mycol Soc 89:483

    Google Scholar 

  • Swart L, Crous PW, Kang JC, Mchau GRA, Pascoe I, Palm ME (2001) Differentiation of species of Elsinoё associated with scab disease of Proteaceae based on morphology, symptomatology, and ITS sequence phylogeny. Mycologia 93:366–379

    Google Scholar 

  • Sweetwood G, Lücking R, Nelsen MP, Aptroot A (2012) Ascospore ontogeny and discharge in megalosporous Trypetheliaceae and Graphidaceae (Ascomycota: Dothideomycetes and Lecanoromycetes) suggest phylogenetic relationships and ecological constraints. Lichenologist 44:277–296

    Google Scholar 

  • Swinscow TDV (1965) Pyrenocarpous lichens: 9. Notes on various species. Lichenologist 3:72–83

    Google Scholar 

  • Swinscow TDV (1970) Pyrenocarpous lichens: 14. Arthopyrenia Massal. sect. Acrocordia (Massal.) Müll. Arg. in the British Isles. Lichenologist 4:218–233

    Google Scholar 

  • Swofford DL (2002) PAUP: phylogenetic analysis using parsimony, version 4.0 b10. Sinauer Associates, Sunderland

  • Sydow H (1925) Fungi in itinere costaricensi collecti. Pars prima. Ann Mycol 23:308–429

    Google Scholar 

  • Sydow H (1953) Fungi venezuelani–Additamentum. Ann Mycol 33:85–100

    Google Scholar 

  • Sydow H, Sydow P (1912) Beschreibungen neuer südafrikanischer. Ann Mycol 10:33–45

    Google Scholar 

  • Sydow H, Sydow P (1916) Weitere Diagnosen neuer philippinischer Pilze. Ann Mycol 14:353–375

    Google Scholar 

  • Takashi Y, Sano A, Yarita K, Suh MK, Nishimura K, Udagawa S (2006) A new species of Cephalotheca isolated from a Korean patient. Mycotaxon 96:309–322

    Google Scholar 

  • Tam WY, Pang KL, Jones EBG (2003) Ordinal placement of selected marine Dothideomycetes inferred from SSU ribosomal DNA sequence analysis. Bot Mar 4:487–494

    Google Scholar 

  • Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28(10):2731–2739

    Google Scholar 

  • Tanaka K, Harada Y (2003a) Pleosporales in Japan (1): the genus Lophiostoma. Mycoscience 44:85–96

    Google Scholar 

  • Tanaka K, Harada Y (2003b) Pleosporales in Japan (2): Lophiotrema. Mycoscience 44:115–121

    Google Scholar 

  • Tanaka K, Harada Y (2003c) Pleosporales in Japan (3). The genus Massarina. Mycoscience 44:173–185

    Google Scholar 

  • Tanaka K, Harada Y (2005) Bambusicolous fungi in Japan (6): Katumotoa, a new genus of phaeosphaeriaceous ascomycetes. Mycoscience 46:313–318

    Google Scholar 

  • Tanaka K, Hosoya T (2008) Lophiostomasagittiforme sp. nov., a new ascomycete (Pleosporales, Dothideomycetes) from Island Yakushima in Japan. Sydowia 60:131–145

    Google Scholar 

  • Tanaka K, Ooki Y, Hatakeyama S, Harada Y, Barr ME (2005) Pleosporales in Japan (5): Pleomassaria, Asteromassaria, and Splanchnonema. Mycoscience 46:248–260

    Google Scholar 

  • Tanaka K, Hirayama K, Yonezawa H, Hatakeyama S, Harada Y, Sano T, Shirouzu T, Hosoya T (2009) Molecular taxonomy of bambusicolous fungi: Tetraplosphaeriaceae, a new pleosporalean family with Tetraploa–like anamorphs. Stud Mycol 64:175–209

    CAS  PubMed Central  PubMed  Google Scholar 

  • Tanaka K, Mel’nik VA, Kamiyama M, Hirayama K, Shirouzu T (2010) Molecular phylogeny of two coelomycetous fungal genera with stellate conidia, Prosthemium and Asterosporium, on Fagales trees. Botany 88:1057–1071

    CAS  Google Scholar 

  • Taylor JE, Groenewald JZ, Crous PW (2003) A phylogenetic analysis of Mycosphaerellaceae leaf spot pathogens of Proteaceae. Mycol Res 107(6):653–658

    CAS  PubMed  Google Scholar 

  • Tehler A (1990) A new approach to the phylogeny of Euascomycetes with a cladistic outline of Arthoniales focussing on Roccellaceae. Can J Bot 68(11):2458–2492

    Google Scholar 

  • Tehler A (1995) Morphological data, molecular data, and total evidence in phylogenetic analysis. Can J Bot 73(suppl 1):S667–S676

    Google Scholar 

  • Tendulkar JS (1971) Mode of sexual reproduction and early development in Parodiella paraguyensis Speg. Nova Hedwigia 21:269–277

    Google Scholar 

  • Teng SC (1933) Notes on Hysteriales from China. Sinensia 4:129–144

    Google Scholar 

  • Teodoro MG, Ferreira MA, Guimarães LMS, Mafia RG, Groenewald JZ, Crous PW, Alfenas AC (2012) Mycosphaerella and Teratosphaeria species associated with leaf diseases on Eucalyptus globulus in southern Brazil. Phytopathol Mediterr 51:355–364

    Google Scholar 

  • Theissen F (1914a) Annotacöes á mycoflora Brasileira. Broteria 12:13–31

    Google Scholar 

  • Theissen F (1914b) Die Trichothyriaceen. Beihefte Botanischen Zentralbl 32(Abt. II):1–16

    Google Scholar 

  • Theissen F (1916) Mykologische Abhandlungen. Verh K-Kg Zool-Botanischen Ges Wien 66:296–400

  • Theissen F, Sydow H (1915) Die Dothideales. Kritisch-systematische riginaluntersuchungen. Ann Mycol 13:147–746

    Google Scholar 

  • Theissen F, Sydow H (1917) Synoptische Tafeln. Ann Mycol 15:389–491

    Google Scholar 

  • Theissen F, Sydow H (1918) Vorentwurfe zu den Pseudosphaeriales. Ann Mycol 16:1–34

    Google Scholar 

  • Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic acids research 25(24):4876

  • Tilak ST (1963) Ascomycetes on Celastrus paniculata Willd. Mycopatholgia 21:60–63

    Google Scholar 

  • Timmer LW, Priest M, Broadbent P, Tan MK (1996) Morphological and pathological characterization of species of Elsinoё causing scab diseases of Citrus. Phytopathology 86:1032–1038

    Google Scholar 

  • Tode HJ (1784) Beschreibung des Venusschwammes (Hysterium). Schriften Berl Ges Naturforschender Freunde 5:53–55

    Google Scholar 

  • Tode HJ (1790) Fungi Mecklenburgenses Selecti. Fasc. 1. Nova Fungorum Genera Complectens. i-viii, 1–50, plates 1–7

  • Tomaselli R, Ciferri R (1952) Scissioni di generi di licheni sulla base delle caratteristiche del fungo. Arch Bot Ital 28:1–15

    Google Scholar 

  • Toro RA (1926) Mixomicetos de Santo Domingo coleccionados por F. D. Kern y R. A. Toro Estacion Agronomica de Haina, Serie B, Botanica 6. pp 7

  • Toro RA (1952) A study of the tropical American black–mildews. J Agric Univ P R 36:24–87

    Google Scholar 

  • Toxopeus J, Kozera CJ, O’Leary SJB, Garbary DJ (2011) A reclassification of Mycophycias ascophylli (Ascomycota) based on nuclear large ribosomal subunit DNA sequences. Bot Mar 54:325–334

    Google Scholar 

  • Tretiach M, Modenesi P (1999) Critical notes on the lichen genus Encephalographa A. Massal. (Hysteriaceae). Nova Hedwigia 68:527–544

    Google Scholar 

  • Triebel D (1989) Lecideicole Ascomyceten. Eine Revision der obligat lichenicolen Ascomyceten auf lecideoiden Flechten. Bibliotheca Lichenologica, No. 35. J. Cramer, Berlin–Stuttgart p 278

  • Tsui CKM, Berbee ML (2006) Phylogenetic relationships and convergence of helicosporous fungi inferred from ribosomal DNA sequences. Mol Phyl Evol 39:587–597

    CAS  Google Scholar 

  • Tsui CKM, Sivichai S, Berbee ML (2006) Molecular systematics of Helicoma, Helicomyces and Helicosporium and their teleomorphs inferred from rDNA sequences. Mycologia 98:94–104

    CAS  PubMed  Google Scholar 

  • Tsui CKM, Sivichai S, Rossman AY, Berbee ML (2007) Tubeufia asiana, the teleomorph of Aquaphila albicans in the Tubeufiaceae, Pleosporales, based on cultural and molecular data. Mycologia 99:884–894

    CAS  PubMed  Google Scholar 

  • Tsuneda A, Hambleton S, Currah RS (2004) Morphology and phylogenetic placement of Endoconidioma, a new endoconidial genus from trembling aspen. Mycologia 96:1128–1135

    CAS  PubMed  Google Scholar 

  • Tsuneda A, Davey ML, Tsuneda I, Currah RS (2010) Two new dothideomycetous endoconidial genera from declining larch. Botany 88:471–487

    Google Scholar 

  • Tucker SC, Harris RC (1980) New or noteworthy pyrenocarpous lichens from Louisiana and Florida. Bryologist 83:1–20

    Google Scholar 

  • Tulasne LR, Tulasne C (1863) Selecta Fungorum Carpologia, vol. 2, 319 pages, 34 Pl. Paris

  • Tulasne LR, Tulasne C (1931) Selecta Fungorum Carpologia of the brothers L. R. and C. Tulasne. Translated into English by W. B. Grove. In: Reginald Buller AH, Shear CL (eds) Volume two [1863]: Xylariei. Valsei. Sphaeriei. With thirty four copper plates. Oxford

  • Ullasa BA (1969) Ascospore germination in Parodiella. Trans Br Mycol Soc 53:319–321

    Google Scholar 

  • Vainio E (1921) Lichenes ab A. Yasuda in Japonia collecti. Continuatio I. Bot Mag (Tokyo) 25:45–79

    Google Scholar 

  • van der Aa HA, Noordeloos ME, DE Gruyter J (1990) Species concepts in some larger genera of the coelomycetes. Stud Mycol 32:3–19

    Google Scholar 

  • van der Linde EJ (1992) Notes on the South African Hysteriaceae (Ascomyctes: Mycotina). S Afr J Bot 58:491–499

    Google Scholar 

  • van Geel B, Buurman J, Brinkkemper O, Schelvis J, Aptroot A, van Reenen G, Hakbijl T (2003) Environmental reconstruction of a Roman Period settlement site in Uitgeest (The Netherlands), with special reference to coprophilous fungi. J Archaeol Sci 30:873–883

    Google Scholar 

  • van Niekerk JM, Crous PW, Groenewald JZ, Fourie PH, Halleen F (2004) DNA phylogeny, morphology and pathogenicity of Botryosphaeria species on grapevines. Mycologia 96:781–798

    PubMed  Google Scholar 

  • van Ryckegem G, Aptroot A (2001) A new Massarina and a new Wettsteinina (Ascomycota) from freshwater and tidal reeds. Nova Hedwigia 73:161–166

    Google Scholar 

  • van Warmelo KT (1966) The identity of a pea blight fungus in South Africa. Bothalia 9:183–194

    Google Scholar 

  • van Wyk PS, Marasas WFO, Hattingh MJ (1976) Morphology and taxonomy of Vizella interrupta (Ascomycetes: Vizellaceae). Trans Br Mycol Soc 66:489–494

    Google Scholar 

  • Vasilyeva LN (2000) Hysteriaceous fungi in the Russian Far East III. Glonium and Actidiographium. Mikol Fitopatol 34:3–5

    Google Scholar 

  • Vasilyeva LN (2001) Hysteriaceous fungi in the Russian Far East IV. Glyphium, Lophium and Mytilinidion. Mikol Fitopatol 35:15–18

    Google Scholar 

  • Verkley GJM, Priest MJ (2000) Septoria and similar coelomycetous anamorphs of Mycosphaerella. Stud Mycol 45:123–128

    Google Scholar 

  • Verkley GJM, Starink-Willemse M, Van Iperen A, Abeln ECA (2004) Phylogenetic analyses of Septoria species based on the ITS and LSU–D2 regions of nuclear ribosomal DNA. Mycologia 96:558–571

    CAS  PubMed  Google Scholar 

  • Verkley GJM, Quaedvlieg W, Shin H-D, Crous PW (2013) A new approach to species delimitation in Septoria. Stud Mycol 75:213–305

    Google Scholar 

  • Vézda A (1975) Foliikole Flechten aus Tanzania (Ost–Afrika). Folia Geobotanica Phytotaxonomica 10:383–432

    Google Scholar 

  • Vézda A (1984) Foliikole Flechten der Insel Kuba. Springer 19(2):177–210

    Google Scholar 

  • Vézda A (2004) Neue foliicole Flechten III. Acta Musei Richnoviensis. Sect Natur 11:57–72

    Google Scholar 

  • Vidal P, Vinuesa MA, Sánchez-Puelles JM, Guarro J (2000) Phylogeny of the anamorphic genus Chrysosporium and related taxabased on rDNA internal transcribed spacer sequences. Rev Iberoam Micol 17:22–29

    Google Scholar 

  • Viegas AP (1943) Piedraia Hortai (Brumpt) Fonseca & Area Leao. Bragantia 3:37–40

    Google Scholar 

  • Voglmayr H, Jaklitsch WM (2011) Molecular data reveal high host specificity in the phylogenetically isolated genus Massaria (Ascomycota, Massariaceae). Fungal Divers 46:133–170

    Google Scholar 

  • Von Arx JA (1952) Studies on Venturia and related genera. Tijdschr Plantenziekten 58:260–266

    Google Scholar 

  • von Arx JA (1963) Die Gattungen der Myriangiales. Persoonia 2(4):421–475

    Google Scholar 

  • von Arx JA (1971) Testudinaceae, a new family of Ascomycetes. Persoonia 6:365–369

    Google Scholar 

  • von Arx JA, Müller E (1954) Die Gattungen der amerosporen Pyrenomyceten. Beitr Kryptogamenflora Schweiz 11:1–434

    Google Scholar 

  • von Arx JA, Müller E (1975) A re-evaluation of the bitunicate Ascomycetes with keys to families and genera. Stud Mycol 9:1–159

    Google Scholar 

  • von Arx JA, van der Aa HA (1983) Notes on Curreya (Ascomycetes, Dothideales). Sydowia 36:1–5

    Google Scholar 

  • Von Höhnel F (1905) Mycologische Fragmente. LXXVII-XCVII. Ann Mycol 3:323–339

    Google Scholar 

  • von Höhnel FXR (1909a) Fragmente zur Mykologie: VII. Mitteilung (Nr. 289 bis 353). Sber Akad Wiss Wien Math–Naturw K l(118):847–848

    Google Scholar 

  • von Höhnel FXR (1909b) Fragmente zur Mykologie VIII. Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse, Abt 1(118):1157–1246

  • von Höhnel FXR (1909c) Fragmente zur Mykologie: VI. Mitteilung (Nr. 182 bis 288). Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse, Abt I. 118:275–452

  • von Höhnel FXR (1910a) Fragmente zur Mykologie: X. Mitteilung (Nr. 468 bis 526). Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften Math.–naturw. Klasse Abt. I, 119:393–473

  • von Höhnel F (1910b) Fragmente zur Mykologie: X. Mitteilung (Nr. 468 bis 526). Sber Akad Wiss Wien Math Naturw Kl 119:393–473

  • von Höhnel FXR (1911) Fragmente zur Mykologie (XIII. Mitteilung, Nr. 642 bis 718). Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse. I. 120:379–384

  • von Höhnel FXR (1917) System der Phacidiales v. H. Sonderabdruck. Ber Dtsch Bot Ges 25:416–422

    Google Scholar 

  • von Höhnel FXR (1918a) Mycologische Fragmente, 272. Über die Hysteriaceen. Ann Mycol 16:145–154

    Google Scholar 

  • von Höhnel FXR (1918b) Fragmente zur Mykologie. Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in WienMathematische–Naturwissenschaftliche Klasse, Abt. 1(127):329–393

  • von Höhnel FXR (1919) Fragmente zur Mykologie. XXII Mitteilungen, nr. 1092 bis 1153. Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse, Abt 1(128):549–634

  • von Höhnel FXR (1928) In Saccardo, Leptopeltineae v. H Syll fung (Abellini) 24(2):1255

  • von Keissler K (1934) Moriolaceae, Epigloeaceae. In: Rabenhorst GL, Kryptogamen–Flora von Deutschland, Österreich und der Schweiz. 2nd IX, Die Flechten, Abt. 1 (2). Borntraeger\Leipzig, pp 1–43

  • von Thümen F (1877) Symbolaead floram mycologicam austriacam. Österr Bot Z 27:270–272

    Google Scholar 

  • Wakefield EM (1940) Nomina generica conservanda. Contributions from the Nomenclature Committee of the British Mycological Society. III. Trans Br Mycol Soc 24:282–293

    Google Scholar 

  • Wang HK, Aptroot A, Crous PW, Hyde KD, Jeewon R (2007) The polyphyletic nature of Pleosporales: an example from Massariosphaeria based on rDNA and RBP2 gene phylogenies. Mycol Res 111:1268–1276

    CAS  PubMed  Google Scholar 

  • Watson W (1929) The classification of lichens. New Phytol 28:85–115

    Google Scholar 

  • Webster J (1956) Conidia of Acrospermum compressum and A. graminum. Trans Br Mycol Soc 39(3):361–366

    Google Scholar 

  • Webster J (1992) Anamorph–teleomorph relationships. In: Bärlocher F (ed) The ecology of aquatic hyphomycetes. Springer–Verlag 99–117

  • Wehmeyer LE (1941) A revision of Melanconis, Pseudovalsa, Prosthecium, and Titania. University of. Mich Stud: Sci Ser 14:1–161

    Google Scholar 

  • Wehmeyer LE (1948) The developmental pattern within the genus Pleospora Rab. Mycologia 40:269–294

    Google Scholar 

  • Wehmeyer LE (1957) The genus Montagnula Berl. Sydowia 1:257–263

    Google Scholar 

  • Wehmeyer LE (1961) A world monograph of the genus Pleospora and its segregates. University of Michigan, Ann Arbor, p 451

    Google Scholar 

  • Wehmeyer LE (1975) The pyrenomycetous fungi. Mycologia Memoir No. 6. The New York Botanical Garden. J. Cramer Publishing, Germany

    Google Scholar 

  • Welch DS (1926) A monographic study of genus Cucurbitaria in North America. Mycologia 1851–86

  • Wiens JJ (2006) Missing data and the design of phylogenetic analyses. J Biomed Inform 39:34–42

    Google Scholar 

  • Wijayawardene DNN, McKenzie EHC, Hyde KD (2012) Towards incorporating anamorphic fungi in a natural classification checklist and notes for 2011. Mycosphere 3:157–228

    Google Scholar 

  • Wijayawardene DNN, Song Y, Bhat DJ, McKenzie EHC, Chukeatirote E, Wang Y, Hyde KD (2013) Wojnowicia viburni sp. nov. from China and its phylogenetic placement. Sydowia 65(1):113–128

  • Wikee S, Udayanga D, Crous PW, Chukeatirote E, McKenzie EHC, Bahkali AH, Dai DQ, Hyde KD (2011) Phyllosticta an over–view of current status of species recognition. Fungal Divers 51:43–61

    Google Scholar 

  • Wikee S, Lombard L, Nakashima C, Motohashi K, Chukeatirote E, Cheewangkoon R, McKenzie EHC, Hyde KD, Crous PW (2013) A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales). Studies in Mycology 76:1–29

    Google Scholar 

  • Willoughby LG, Archer JF (1973) The fungal spora of a freshwater stream and its colonization pattern on wood. Freshw Biol 3:219–239

    Google Scholar 

  • Wingfield MJ, de Beer ZW, Slippers B, Wingfield BD, Groenewald JZ et al (2012) One fungus one name promotes progressive plant pathology. Mol Plant Pathol 13:604–613

    CAS  PubMed  Google Scholar 

  • Winka K, Eriksson OE, Bäng A (1998) Molecular evidence for recognizing the Chaetothyriales. Mycologia 90:822–830

    CAS  Google Scholar 

  • Winter G (1885) Pilze–Ascomyceten. In: GL Rabenhorst’s Kryptogamen–Flora von Deutschland, Oesterreich und der Schweiz. 1:65–528

  • Winter G (1887) Ascomyceten. Rab Krypt Flora 1(2):1–928

    Google Scholar 

  • Wolf FA, Wolf FT (1947). The Fungi 1: 438 pp., 153 figs. USA, New York; UK, London; Wiley, Chapman & Hall

  • Wong MH, Crous PW, Henderson J, Groenewald JZ, Drenth A (2012) Phyllosticta species associated with freckle disease of banana. Fungal Divers 56:173–187

    Google Scholar 

  • Woronichin NN (1915) Les fumagines de Sotschi. Bull Appl Bot 8:769–807

    Google Scholar 

  • Woronichin NN (1925) Über die Capnodiales. Ann Mycol 23:174–178

    Google Scholar 

  • Woronichin NN (1926) Zur Kenntnis der Morphologie und Systematik der Russtaupilze Transkaukasiens. Ann Mycol 24:231–264

    Google Scholar 

  • Woudenberg JHC, Groenewald JZ, Binder M, Crous PW (2013) Alternaria redefined. Stud Mycol 75:171–212

    CAS  PubMed Central  PubMed  Google Scholar 

  • Wu HX, Jaklitsch WM, Voglmayr H, Hyde KD (2011a) Epitypification, morphology and phylogeny of Tothi fuscella. Mycotaxon 118:203–211

    Google Scholar 

  • Wu HX, Schoch CL, Boonmee S, Bahkali AH, Chomnunti P, Hyde KD (2011b) A reappraisal of Microthyriaceae. Fungal Divers 51(1):189–248

    PubMed Central  PubMed  Google Scholar 

  • Wulandari NF, To-anun C, Hyde KD, Duong LM, de Gruyter J et al (2009) Phyllosticta citriasiana sp. nov. the cause of Citrus tan spot of Citrus maxima in Asia. Fungal Divers 34:23–39

    Google Scholar 

  • Yao YJ, Spooner BM (1999) Roesleriaceae, a new family of Ascomycota, and a new species of Roeslerina. Kew Bull 54:683–693

    Google Scholar 

  • Yarwood CE (1973) Pyrenomycetes: Erysiphales. In: Ainsworth GC, Sparrow FK, Sussman A (eds) The fungi, vol. IVA. Academic, New York, pp 71–86

    Google Scholar 

  • Yeshitela K, Fischer E, Killmann D, Sérusiaux E (2009) Aspidothelium hirsutum (Thelenellaceae) and Caprettia goderei (Monoblastiaceae), two new species of foliicolous lichens from Ethiopia and Kenya. Bryologist 112:850–855

    Google Scholar 

  • Zahlbruckner A (1898) Beiträge zur Flechtenflora Niederösterreichs V. Verhandlungen der Kaiserlich-Königlichen Zoologisch-Botanischen Gesellschaft in Wien 48:349–370

  • Zahlbruckner A (1903) Lichenes, Spezieller Teil. In: Engler A, Prantl K (eds) Die Naturlichen Pflanzenfamilien, Abt. 1, t. 1. Engelmann, Leipzig. 49–249

  • Zahlbruckner A (1907) Mastodiaceae. In: Engler HGA, PrantlK AE (eds) Die natürlichen Pflanzenfamilien nebst ihren Gattungen und wichtigeren Arten insbesondere den Nutzpflanzen, unter Mitwirkung zahlreicher hervorragender Fachgelehrten I. Abteilung 1:240. Leipzig, Germany

  • Zahlbruckner A (1926) Catalogus Lichenum Universalis. Borntraeger, Leipzig

    Google Scholar 

  • Zahlbruckner A (1935) Florida–Flechten, gesammelt von S. Rapp. Ann Mycol 33:33–45

    Google Scholar 

  • Zalasky H (1968) Rhytidiella moriformis n. gen., n. sp. causing rough–bark of Populus balsamifera. Can J Bot 46:1383–1387

    Google Scholar 

  • Zenker JK (1827) Lichenes. In: Goebel F, Kunze G (eds) Pharmazeutische Waarenkunde 1:109–199. Eisenach

  • Zhang M, Koko TW, Hyde KD (2011a) Towards a monograph of Dothideomycetes: Studies on Diademaceae. Cryptogam Mycol 32:115–126

    Google Scholar 

  • Zhang Y, Hyde KD (2009) Transfer of Pseudoparodia pseudopeziza to Patellariaceae (Patellariales). Nova Hedwigia 88:211–215

    Google Scholar 

  • Zhang Y, Fournier J, Pointing SB, Hyde KD (2008a) Are Melanomma pulvis–pyrius and Trematosphaeria pertusa congeneric? Fungal Divers 33:47–60

    CAS  Google Scholar 

  • Zhang Y, Jeewon R, Fournier J, Hyde KD (2008b) Multi–gene phylogeny and morphotaxonomy of Amniculicola lignicola: a novel freshwater fungus from France and its relationships to the Pleosporales. Mycol Res 112:1186–1194

    CAS  PubMed  Google Scholar 

  • Zhang Y, Fournier J, Crous PW, Pointing SB, Hyde KD (2009a) Phylogenetic and morphological assessment of two new species of Amniculicola and their allies (Pleosporales). Persoonia 23:48–54

    PubMed Central  PubMed  Google Scholar 

  • Zhang Y, Schoch CL, Fournier J, Crous PW, de Gruyter J, Woudenberg JHC, Hirayama K, Tanaka K, Pointing SB, Spatafora JW, Hyde KD (2009b) Multi–locus phylogeny of Pleosporales: a taxonomic, ecological and evolutionary re–evaluation. Stud Mycol 64:85–102

    CAS  PubMed Central  PubMed  Google Scholar 

  • Zhang Y, Wang HK, Fournier J, Crous PW, Jeewon R, Pointing SB, Hyde KD (2009c) Towards a phylogenetic clarification of Lophiostoma, Massarina and morphologically similar genera in the Pleosporales. Fungal Divers 38:225–251

    Google Scholar 

  • Zhang Y, Crous PW, Schoch CL, Bahkali AH, Guo LD, Hyde KD (2011b) A molecular, morphological and ecological re-appraisal of Venturiales-a new order of Dothideomycetes. Fungal Divers 51:249–277

    PubMed Central  PubMed  Google Scholar 

  • Zhang Y, Crous PW, Schoch CL, Hyde KD (2012a) Pleosporales. Fungal Divers 53:1–221

    CAS  PubMed Central  PubMed  Google Scholar 

  • Zhang Y, Fournier J, Phookamsak R, Bakhali AH, Hyde KD (2012b) Halotthiaceae fam. nov. (Ploepsorales) accommodates the new genus Phaeoseptum and several other aquatic genera. Mycologia 40:107–110

    Google Scholar 

  • Zhang Y, Fournier J, Phookamsak R, Bahkali Ali H, Hyde KD (2013) Halotthiaceae fam. nov. (Pleosporales) accommodates the new genus Phaeoseptum and several other aquatic genera. Mycologia 105:603–609

    PubMed  Google Scholar 

  • Zhaxybayeva O, Gogarten JP (2002) Bootstrap, Bayesian probability and maximum likelihood mapping: exploring new tools for comparative genome analyses. BMC Genomics 3(1):4

    Google Scholar 

  • Zhuang WY, Liu CY (2012) What an rRNA secondary structure tells about phylogeny of fungi in Ascomycota with emphasis on evolution of major types of ascus. PLoS One 7:e47546

    CAS  PubMed Central  PubMed  Google Scholar 

  • Zogg H (1962) Die Hysteriaceae s. str. und Lophiaceae, unter besonderer Berücksichtigung der mitteleuropäischen Formen. Beitr Kryptogamenflora Schweiz Band 11:1–190

    Google Scholar 

  • Zukal H (1890) Epigloea bactrospora. Eine neue Gallertflechte mit chlorophyllhältigen

Download references

Acknowledgments

The curators of the herbarium ANM, AR, B, BBH, BCC, BISH, BP, BPI, BR, BRIP, CBS, DAOM, FH, G, GZU, GZU, H, HAL, HHUF, HKU(M), IFRD, ILLS, IMI, K, L, LPS, MFU, NY, P, PREM, S, TRTC, UBC, UC, UCR, UPS, URM, URM and W are especially thanked for sending and loaning herbarium specimens and for being very helpful when it came to locating specimens. Without their help this work would not have been possible. The abbreviations of herbarium are those listed in Index Herbariorum (2013). We also thank Siriporn Luesuwan for arranging the loan of specimens from various herbaria.

A. Ariyawansa and J.C Kang are grateful to the International collaboration plan of Science and Technology at Guizhou Province (contract No. [2012] 7006) and the construction of innovation talent team of Science and Technology at Guizhou Province (contract No. [2012]4007), China. D.J. Bhat is thankful to MFU for a Visiting Professorship during the tenure of which this paper was finalized. D.L.Hawksworth contributed to this work while in receipt of support from the Spanish Ministerio de Ciencia e Innovación (CGL2011-25003). Haixia Wu would like to thank the Grant for Essential Scientific Research of National Non–profit Institute to funds for research (No. CAFYBB2007002) and thanks Xiaoming Chen, Ying Feng and Chen Hang (The Research Institute of Resource Insects, Chinese Academy of Forestry, China) for their valuable help. Jian-Kui Liu would like to thank Manfred Binder for providing valuable suggestions and kind assistance on phylogenetic analysis. We would like to thank MFU grant No. 56101020032 for funding to study taxonomy and phylogeny of selected families of Dothideomycetes. Jiye Yan and Xinghong Li would like to thank CARS-30 for funds. K. Tanaka would like to thank the Japan Society for the Promotion of Science (JSPS, 25440199) for financial support. K.L. Pang would like to thank National Science Council of Taiwan for financial support (NSC101–2621–B–019–001–MY3). L. Muggia is grateful to the Austrian Science Foundation for financial support (FWF, P24114-B16 and Herta-Firnberg Project T481-B20). M. Doilom would like to thank the Thailand Research Fund through the Royal Golden Jubilee (RGJ) Ph.D. Program grant No. Ph.D./0072/2553 in 4.S.M.F./53/A.2. MP Nelsen and R Lücking are grateful to the NSF (DEB 0715660 “Neotropical Epiphytic Microlichens - An Innovative Inventory of a Highly Diverse yet Little Known Group of Symbiotic Organisms”; DEB 0717476 “Systematics of Dothideomycetes”); MP Nelsen also acknowledges a Brown Family Fellowship through the Field Museum, a William Harper Rainey Fellowship through the University of Chicago, and support through the Committee on Evolutionary Biology at the University of Chicago. R. Phookamsak would like to thank the Royal Golden Jubilee Ph. D. Program (PHD/0090/2551) under the Thailand Research Fund for scholarship support. S. A. Alias would like to thank Program Rakan University Malaya (PRPUM) - Phylogeny, Taxonomy, Relationships and Biotechnological Potential of Sooty Moulds. S. Boonmee also thanks Amy Y. Rossman and the U.S. Department of Agriculture Agricultural Research Service, Systematic Mycology and Microbiology Lab (SMML), USA for laboratory, funding support and advice on her work. S. Boonmee and P. Chomnunti would like to thank TRF/BIOTEC program Biodiversity Research and Training Grant BRT R_251181, BRT R_253012 and the Mushroom Research Foundation, Chiang Rai Province for funding support. S. Wikee would like to thank the Thailand Research Fund through the Royal Golden Jubilee Ph.D. Program agreement No PhD/0198/2552. S. Wikee and JK Liu would like to thank The National Research Council of Thailand (NRCT) for the award of grant No 55201020002 to study the genus Phyllosticta in Thailand. S. Suetrong acknowledges the financial support by TRF/BIOTEC program Biodiversity Research and Training Grant BRT R_351004 and BRT R_325015 to study marine fungi of Thailand. Suetrong also thanks Morakot Tanticharoen, Kanyawim Kirtikara and Lily Eurwilaichitr, BIOTEC, Bangkok for their continued interest and support. Supalak Yacharoen, J. Monkai and K.D. Hyde would like to thank the Thailand Research Fund (BRG5280002) for financial support. Gareth Jones is supported by the Distinguished Scientist Fellowship Program (DSFP), King Saud University, Saudi Arabia. Y. Wang would like to thank The International Scientific Cooperated Project of Guizhou Province (No [2013]7004). Yongxiang Liu would like to thank the Guizhou Research Fund (QKHZYZ[2010]5031 and QNKYYZX[2012]010) for financial support. Harrie Sipman is thanked for comments on part of the manuscript.

Author information

Authors and Affiliations

  1. Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming, 650201, Yunnan, China

    Kevin D. Hyde, Peter E. Mortimer & Jian-Chu Xu

  2. World Agroforestry Centre, East Asia Node, Heilongtan, Kunming, 650201, China

    Kevin D. Hyde & Peter E. Mortimer

  3. Institute of Excellence in Fungal Research, Chiang Rai, 57100, Thailand

    Kevin D. Hyde, Jian-Kui Liu, Hiran Ariyawansa, Saranyaphat Boonmee, Putarak Chomnunti, Dong-Qin Dai, Asha Dissanayake, Mingkhuan Doilom, Singang Hongsanan, Ruvishika Jayawardena, Jutamart Monkai, Rungtiwa Phookamsak, Indunil C. Senanayake, Kasun M. Thambugala, Nalin N. Wijayawardene, Saowanee Wikee, Ekachai Chukeatirote, Wen-Jing Li, Ausana Mapook, Qing Tian, Saowaluck Tibpromma, Dhanushka N. Wanasinghe & Supalak Yacharoen

  4. School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand

    Kevin D. Hyde, Jian-Kui Liu, Hiran Ariyawansa, Saranyaphat Boonmee, Putarak Chomnunti, Dong-Qin Dai, Asha Dissanayake, Mingkhuan Doilom, Singang Hongsanan, Ruvishika Jayawardena, Jutamart Monkai, Rungtiwa Phookamsak, Indunil C. Senanayake, Kasun M. Thambugala, Nalin N. Wijayawardene, Saowanee Wikee, D. Jayarama Bhat, Ekachai Chukeatirote, Wen-Jing Li, Ausana Mapook, Qing Tian, Saowaluck Tibpromma, Dhanushka N. Wanasinghe & Supalak Yacharoen

  5. Institute Ocean Earth Sciences, Kuala Lumpur, 50603, Selangor, Malaysia

    E. B. Gareth Jones

  6. Department of Botany and Microbiology, King Saudi University, Riyadh, Saudi Arabia

    E. B. Gareth Jones

  7. 42 Longacre Drive, Livingston, NJ, 07039, USA

    Eric Boehm

  8. Institut für Biologie, Bereich Geobotanik und Botanischer Garten, Herbarium, Martin-Luther-Universität, Neuwerk 21, 06099, Halle (Saale), Germany

    Uwe Braun

  9. CBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands

    Pedro W. Crous & Sybren De Hoog

  10. Musée National d’histoire Naturelle, 25 rue Munster, 2160, Luxembourg, Luxembourg

    Paul Diederich

  11. Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences, Beijing, 100097, People’s Republic of China

    Asha Dissanayake, Ruvishika Jayawardena, Xing-Hong Li & Ji-Ye Yan

  12. Via dei Funaioli 22, 57126, Livorno, Italy

    Francesco Doveri

  13. Department of Environmental Science and Policy, George Mason University, 4400 University Drive, Fairfax, VA, 22030-4444, USA

    James D. Lawrey

  14. International Fungal Research and Development Centre, Key Laboratory of Resource Insect Cultivation & Utilization State Forestry Administration, Kunming, 650224, People’s Republic of China

    Yan-Mei Li, Hai-Xia Wu & Min Zhang

  15. The Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, 650224, People’s Republic of China

    Yan-Mei Li, Hai-Xia Wu & Min Zhang

  16. Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Guiyang, Guizhou, 550006, People’s Republic of China

    Yong-Xiang Liu, Kasun M. Thambugala & Zou-Yi Liu

  17. Science and Education, Integrative Research (Botany), The Field Museum, 1400 South Lake Shore Drive, Chicago, IL, 60605-2496, USA

    Robert Lücking & Matthew P. Nelsen

  18. Institute of Plant Sciences, University of Graz, Holteigasse 6, 8010, Graz, Austria

    Lucia Muggia & Christian Scheuer

  19. Department of Life Science, University of Trieste, Via L. Giorgieri 10, Trieste, Italy

    Lucia Muggia

  20. Committee on Evolutionary Biology, University of Chicago, 1025 E. 57th Street, Chicago, IL, 60637, USA

    Matthew P. Nelsen

  21. Institute of Marine Biology and Center of Excellence for the Oceans, National Taiwan Ocean University, 2 Pei-Ning Road, Keelung, 20224, Taiwan

    Ka-Lai Pang

  22. Department of Plant Biology, University of Illinois, Rm. 265 Morrill Hall, 505 South Goodwin Avenue, Urbana, IL, 61801, USA

    Carol A. Shearer

  23. Mycology Laboratory, Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), 113 Thailand Science Park, Phahonyothin Road, Khlong Nueng, Khlong Luang, Pathum Thani, 12120, Thailand

    Satinee Suetrong

  24. Faculty of Agriculture and Life Science, Hirosaki University, 3 Bunkyo-cho, Hirosaki, Aomori, 036-8561, Japan

    Kazuaki Tanaka & Kazuyuki Hirayama

  25. Institute of Microbiology, Beijing Forestry University, P.O. Box 61, Beijing, 100083, People’s Republic of China

    Ying Zhang

  26. Mycology Section, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK

    Begoña Aguirre-Hudson & David L. Hawksworth

  27. Institute of Biological Sciences, University of Malaya, 50603, Kuala Lumpur, Malaysia

    S. Aisyah Alias

  28. ABL Herbarium, G.v.d. Veenstraat 107, NL-3762 XK, Soest, The Netherlands

    André Aptroot

  29. College of Science, Botany and Microbiology Department, King Saud University, Riyadh, 1145, Saudi Arabia

    Ali H. Bahkali

  30. Departamento de Micologia, Universidade Federal de Pernambuco Rua Nelson Chaves, s/n, Cidade Universitária, Recife, 50670-901, Brazil

    Jose L. Bezerra

  31. No. 128/1-J, Azad Housing Society, Curca, P.O. Goa Velha, 403108, India

    D. Jayarama Bhat

  32. Department of Botany, Goa University, Goa, 403 206, India

    D. Jayarama Bhat

  33. A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy

    Erio Camporesi

  34. A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy

    Erio Camporesi

  35. Società per gli Studi Naturalistici della Romagna, C.P. 144, Bagnacavallo (RA), Italy

    Erio Camporesi

  36. Department of Life Sciences, The Natural History Museum, Cromwell Road, SW7 5BD, London, UK

    Cécile Gueidan & David L. Hawksworth

  37. Departamento de Biología Vegetal II, Facultad de Farmacia, Universidad Complutense de Madrid, Plaza Ramón y Cajal, Madrid, 28040, Spain

    David L. Hawksworth

  38. The Engineering and Research Center for Southwest Bio-Pharmaceutical Resources of National Education Ministry of China, Guizhou University, Guiyang, 550025, Guizhou Province, People’s Republic of China

    Ji-Chuan Kang

  39. The Herbarium, Department of Botany and Plant Sciences, University of California, Riverside, CA, 92521, USA

    Kerry Knudsen

  40. Manaaki Whenua Landcare Research, Private Bag 92170, Auckland, New Zealand

    Eric H. C. McKenzie

  41. Illinois Natural History Survey, 1816 South Oak Street, Champaign, IL, 61820, USA

    Andrew N. Miller

  42. Centro de Recursos Microbiológicos, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516, Caparica, Portugal

    Alan J. L. Phillips

  43. Department of Chemistry and Biochemistry, University of North Carolina, 457 Sullivan Science Building, Greensboro, NC, 27402-6170, USA

    Huzefa A. Raja

  44. Mozartstr. 9, 73117, Wangen, Germany

    Felix Schumm

  45. Royal Botanic Garden Edinburgh, 20 Inverleith Row, Edinburgh, EH3 5LR, UK

    Joanne E. Taylor

  46. Department of Plant Pathology, Agriculture College, Guizhou University, Guiyang, 550025, People’s Republic of China

    Yong Wang

Authors
  1. Kevin D. Hyde
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. E. B. Gareth Jones
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Jian-Kui Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Hiran Ariyawansa
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Eric Boehm
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Saranyaphat Boonmee
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Uwe Braun
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Putarak Chomnunti
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Pedro W. Crous
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Dong-Qin Dai
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Paul Diederich
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Asha Dissanayake
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Mingkhuan Doilom
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Francesco Doveri
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Singang Hongsanan
    View author publications

    You can also search for this author in PubMed Google Scholar

  16. Ruvishika Jayawardena
    View author publications

    You can also search for this author in PubMed Google Scholar

  17. James D. Lawrey
    View author publications

    You can also search for this author in PubMed Google Scholar

  18. Yan-Mei Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  19. Yong-Xiang Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  20. Robert Lücking
    View author publications

    You can also search for this author in PubMed Google Scholar

  21. Jutamart Monkai
    View author publications

    You can also search for this author in PubMed Google Scholar

  22. Lucia Muggia
    View author publications

    You can also search for this author in PubMed Google Scholar

  23. Matthew P. Nelsen
    View author publications

    You can also search for this author in PubMed Google Scholar

  24. Ka-Lai Pang
    View author publications

    You can also search for this author in PubMed Google Scholar

  25. Rungtiwa Phookamsak
    View author publications

    You can also search for this author in PubMed Google Scholar

  26. Indunil C. Senanayake
    View author publications

    You can also search for this author in PubMed Google Scholar

  27. Carol A. Shearer
    View author publications

    You can also search for this author in PubMed Google Scholar

  28. Satinee Suetrong
    View author publications

    You can also search for this author in PubMed Google Scholar

  29. Kazuaki Tanaka
    View author publications

    You can also search for this author in PubMed Google Scholar

  30. Kasun M. Thambugala
    View author publications

    You can also search for this author in PubMed Google Scholar

  31. Nalin N. Wijayawardene
    View author publications

    You can also search for this author in PubMed Google Scholar

  32. Saowanee Wikee
    View author publications

    You can also search for this author in PubMed Google Scholar

  33. Hai-Xia Wu
    View author publications

    You can also search for this author in PubMed Google Scholar

  34. Ying Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  35. Begoña Aguirre-Hudson
    View author publications

    You can also search for this author in PubMed Google Scholar

  36. S. Aisyah Alias
    View author publications

    You can also search for this author in PubMed Google Scholar

  37. André Aptroot
    View author publications

    You can also search for this author in PubMed Google Scholar

  38. Ali H. Bahkali
    View author publications

    You can also search for this author in PubMed Google Scholar

  39. Jose L. Bezerra
    View author publications

    You can also search for this author in PubMed Google Scholar

  40. D. Jayarama Bhat
    View author publications

    You can also search for this author in PubMed Google Scholar

  41. Erio Camporesi
    View author publications

    You can also search for this author in PubMed Google Scholar

  42. Ekachai Chukeatirote
    View author publications

    You can also search for this author in PubMed Google Scholar

  43. Cécile Gueidan
    View author publications

    You can also search for this author in PubMed Google Scholar

  44. David L. Hawksworth
    View author publications

    You can also search for this author in PubMed Google Scholar

  45. Kazuyuki Hirayama
    View author publications

    You can also search for this author in PubMed Google Scholar

  46. Sybren De Hoog
    View author publications

    You can also search for this author in PubMed Google Scholar

  47. Ji-Chuan Kang
    View author publications

    You can also search for this author in PubMed Google Scholar

  48. Kerry Knudsen
    View author publications

    You can also search for this author in PubMed Google Scholar

  49. Wen-Jing Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  50. Xing-Hong Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  51. Zou-Yi Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  52. Ausana Mapook
    View author publications

    You can also search for this author in PubMed Google Scholar

  53. Eric H. C. McKenzie
    View author publications

    You can also search for this author in PubMed Google Scholar

  54. Andrew N. Miller
    View author publications

    You can also search for this author in PubMed Google Scholar

  55. Peter E. Mortimer
    View author publications

    You can also search for this author in PubMed Google Scholar

  56. Alan J. L. Phillips
    View author publications

    You can also search for this author in PubMed Google Scholar

  57. Huzefa A. Raja
    View author publications

    You can also search for this author in PubMed Google Scholar

  58. Christian Scheuer
    View author publications

    You can also search for this author in PubMed Google Scholar

  59. Felix Schumm
    View author publications

    You can also search for this author in PubMed Google Scholar

  60. Joanne E. Taylor
    View author publications

    You can also search for this author in PubMed Google Scholar

  61. Qing Tian
    View author publications

    You can also search for this author in PubMed Google Scholar

  62. Saowaluck Tibpromma
    View author publications

    You can also search for this author in PubMed Google Scholar

  63. Dhanushka N. Wanasinghe
    View author publications

    You can also search for this author in PubMed Google Scholar

  64. Yong Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  65. Jian-Chu Xu
    View author publications

    You can also search for this author in PubMed Google Scholar

  66. Supalak Yacharoen
    View author publications

    You can also search for this author in PubMed Google Scholar

  67. Ji-Ye Yan
    View author publications

    You can also search for this author in PubMed Google Scholar

  68. Min Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding authors

Correspondence to Kevin D. Hyde or Peter E. Mortimer.

Electronic supplementary material

ESM 1

(DOC 527 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hyde, K.D., Jones, E.B.G., Liu, JK. et al. Families of Dothideomycetes. Fungal Diversity 63, 1–313 (2013). https://doi.org/10.1007/s13225-013-0263-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13225-013-0263-4

Keywords

Search

Navigation